79312036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344392-A-G

79312138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344480-A-T

79312277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344624-A-G

http://identifiers.org/hco/13/GRCh38#79312323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105344670-A-C

79312334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344681-C-T

79312344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344691-T-C

79312378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344723-T-C

79312544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105344899-A-G

79313257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105345620-T-A

79313839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105346196-G-A

79313841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105346198-A-G

79314167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105346482-G-T

http://identifiers.org/hco/13/GRCh38#79314308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105346601-A-C

http://identifiers.org/hco/13/GRCh38#79314701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105346946-C-A

79314940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3 prime UTR variant
orthologous variants: 105347188-G-T

http://identifiers.org/hco/13/GRCh38#79315022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105347271-A-C

79315022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105347271-A-T

79315095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105347343-A-G

79315095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105347343-A-T

http://identifiers.org/hco/13/GRCh38#79315196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105347449-C-A

79315554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105347795-C-T

79315951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348160-G-T

79316139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348363-A-G

79316155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348379-T-C

79316171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348393-T-C

79316231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348407-G-C

79316257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348430-T-C

79316279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348456-T-C

79316324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348497-C-T

79316698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105348900-T-G

79316875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105349028-C-G

79317028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105349170-T-C

http://identifiers.org/hco/13/GRCh38#79318127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105350199-C-A

79318127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105350199-C-T

79318157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105350229-C-T

79318173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105350244-A-G

79318173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105350244-A-T

http://identifiers.org/hco/13/GRCh38#79318237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105350297-C-A

79318237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105350297-C-T

http://identifiers.org/hco/13/GRCh38#79319074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105351132-C-A

79319074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351132-C-T

79319349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351381-T-C

http://identifiers.org/hco/13/GRCh38#79319441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105351463-C-A

http://identifiers.org/hco/13/GRCh38#79319601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105351622-A-C

79319623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351644-A-G

79319832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351843-G-A

79319832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351843-G-T

79319859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351863-G-T

79319896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351900-T-C

79319908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351912-T-C

http://identifiers.org/hco/13/GRCh38#79319974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105351989-A-C

79319974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351989-A-G

79319974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105351989-A-T

http://identifiers.org/hco/13/GRCh38#79320016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105352028-C-A

79320016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352028-C-G

79320016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352028-C-T

79320194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352210-G-C

79320194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352210-G-T

79320211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352227-T-C

79320816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352927-A-G

79320829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105352941-T-C

79321492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105353583-A-G

79321691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105353784-G-C

http://identifiers.org/hco/13/GRCh38#79322170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105354237-C-A

79322170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105354237-C-T

http://identifiers.org/hco/13/GRCh38#79322171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105354238-C-A

79322171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105354238-C-T

79322418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: synonymous variant
orthologous variants: 105354491-C-T

http://identifiers.org/hco/13/GRCh38#79323061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105356119-C-A

79323147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105356207-G-A

http://identifiers.org/hco/13/GRCh38#79323218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105356263-A-C

79323411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105356450-G-C

79323495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105356505-T-C

79323502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105356512-G-T

79323580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105356562-G-A

79333895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105357544-T-G

79334217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358312-T-C

79334235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358330-T-C

79334271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358348-T-C

79334288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358365-A-G

79334395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: synonymous variant
orthologous variants: 105358469-A-G

79334498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358565-T-A

79334611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358633-G-C

79334695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358712-G-A

79334926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105358915-T-G

79335601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105360400-A-G

79335884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105360674-T-A

79335930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105360714-C-T

79336401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105361133-G-A

79336580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105361279-G-C

79336846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105361532-A-G

79336853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105361539-A-G

79336994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105361900-T-C

http://identifiers.org/hco/13/GRCh38#79337197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105362114-C-A

79337197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: missense variant
orthologous variants: 105362114-C-T

79337311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362228-G-C

http://identifiers.org/hco/13/GRCh38#79337386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105362430-C-A

79337490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362518-G-A

79337613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362748-T-A

79337664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362803-C-G

79337664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362803-C-T

79337772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105362921-T-C

79337889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363026-T-C

79337889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363026-T-G

79337938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363115-C-T

79339117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363773-C-T

79339241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363801-T-C

79339281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363841-G-A

79339330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363873-G-C

79339336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105363878-T-C

http://identifiers.org/hco/13/GRCh38#79339494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105363999-C-A

http://identifiers.org/hco/13/GRCh38#79339562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105364065-C-A

79339562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364065-C-T

http://identifiers.org/hco/13/GRCh38#79339742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105364329-C-A

79339805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364386-T-C

79339927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364499-G-A

79340025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364583-C-T

79340218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364773-T-A

79340285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105364835-G-T

79340492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365143-C-T

79340496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365147-T-C

79340545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365197-A-G

79340930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365694-T-G

79341041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365799-G-A

79341041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365799-G-T

79341100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365978-T-C

79341100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105365978-T-G

79341274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366145-G-A

79341274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366145-G-C

79341274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366145-G-T

79341308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366198-G-A

79341308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366198-G-T

79341311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366201-G-T

http://identifiers.org/hco/13/GRCh38#79341379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105366324-C-A

79341379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366324-C-G

79341379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366324-C-T

79341703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366652-G-T

79341946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105366873-G-A

79342182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367099-C-T

79342356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367258-A-G

http://identifiers.org/hco/13/GRCh38#79342472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105367373-C-A

79342472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367373-C-T

79342506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367434-T-A

79342522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367475-A-T

79342533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367486-G-T

79342576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367591-A-G

79342628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367636-A-G

79342628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105367636-A-T

79343319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368248-G-T

79343355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368269-A-G

http://identifiers.org/hco/13/GRCh38#79343489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105368375-A-C

79343831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368541-A-G

79344130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368800-A-G

79344131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368801-T-C

79344157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368827-G-A

79344157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368827-G-C

79344157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368827-G-T

79344172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368842-A-G

79344180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368850-G-A

79344180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368850-G-T

79344191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368862-A-G

http://identifiers.org/hco/13/GRCh38#79344206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105368877-A-C

79344206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105368877-A-G

79344436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369092-G-A

http://identifiers.org/hco/13/GRCh38#79344546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105369181-C-A

79344546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369181-C-T

http://identifiers.org/hco/13/GRCh38#79344655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105369304-C-A

79344655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369304-C-T

79344771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: synonymous variant
orthologous variants: 105369420-T-C

79344802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105369451-T-C

79344808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369457-T-C

79344841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369532-G-C

79344841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369532-G-T

79344889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369582-T-G

http://identifiers.org/hco/13/GRCh38#79344914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105369597-A-C

79344981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369673-G-T

79345075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369760-A-G

http://identifiers.org/hco/13/GRCh38#79345250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105369896-C-A

79345306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105369936-T-G

79345541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105370149-C-G

79345541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105370149-C-T

79345807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105370386-C-T

79346281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105370836-T-C

79346311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105370856-T-C

79346712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371241-T-G

79346887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371389-A-G

79346952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371440-C-T

http://identifiers.org/hco/13/GRCh38#79347106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105371565-C-A

79347169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371623-G-C

79347169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371623-G-T

79347263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105371719-G-A

79347629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105372250-T-C

79347822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105372474-T-G

79348183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105372815-T-C

79348342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105372990-G-A

79348696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105373581-T-G

79349278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105374211-T-C

79349500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105374379-T-C

79351657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105375153-A-G

79352277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105375751-C-T

http://identifiers.org/hco/13/GRCh38#79352478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105375851-A-C

79352721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376094-C-T

http://identifiers.org/hco/13/GRCh38#79352934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376300-A-C

79352989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376354-G-A

http://identifiers.org/hco/13/GRCh38#79353094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376470-A-C

79353094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376470-A-G

79353094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376470-A-T

http://identifiers.org/hco/13/GRCh38#79353131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376508-C-A

79353131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376508-C-T

http://identifiers.org/hco/13/GRCh38#79353133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376510-C-A

79353133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376510-C-T

79353306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376681-T-A

79353306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376681-T-C

79353447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105376845-A-G

http://identifiers.org/hco/13/GRCh38#79353514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376907-A-C

http://identifiers.org/hco/13/GRCh38#79353515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105376908-A-C

79353984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377357-T-C

http://identifiers.org/hco/13/GRCh38#79354182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105377546-A-C

79354375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377686-T-C

79354395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377706-A-G

79354456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: missense variant
orthologous variants: 105377769-A-G

79354478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: synonymous variant
orthologous variants: 105377791-T-C

79354619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377932-G-A

79354619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377932-G-T

79354626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377939-G-A

79354626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105377939-G-T

79354862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105378318-G-A

79354866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105378322-T-C

79355216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105378628-T-C

79355492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105378901-A-T

79358195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105380060-T-C

79358198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105380064-A-G

79358468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105380321-T-C

79359284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381237-T-C

79359286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381239-T-C

http://identifiers.org/hco/13/GRCh38#79359445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105381498-A-C

79359520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381569-A-T

http://identifiers.org/hco/13/GRCh38#79359548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105381588-A-C

79359548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381588-A-G

79359726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381754-G-C

79359726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381754-G-T

http://identifiers.org/hco/13/GRCh38#79359775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105381803-C-A

79359775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105381803-C-T

http://identifiers.org/hco/13/GRCh38#79360734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105382139-A-C

79361311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382427-G-T

79361420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382511-C-T

79361423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382514-T-A

79361536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382609-G-A

79361590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382728-C-T

79361641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382796-T-C

79361824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105382985-C-T

79361860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383009-T-C

79361868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383017-T-A

79361868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383017-T-C

79361917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383076-C-T

79361918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383077-G-A

79361972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383130-G-A

79361972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383130-G-C

http://identifiers.org/hco/13/GRCh38#79362060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105383180-A-C

79362183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383288-T-G

79362220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383326-T-C

79362357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383452-C-T

79362409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383503-T-A

79362706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383769-T-A

79362824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105383863-C-T

79363006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105384013-C-T

79363403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105385442-G-A

79363773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105385736-T-C

http://identifiers.org/hco/13/GRCh38#79364111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105386428-C-A

79364111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105386428-C-T

79364215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105386539-A-G

79364216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105386540-T-G

79364228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105386554-G-A

79364228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105386554-G-C

79366326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388458-T-A

79366326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388458-T-G

79366489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388619-T-C

79366489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388619-T-G

79366501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388631-G-A

79366501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388631-G-C

79366501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388631-G-T

79366504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388634-T-A

79366504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105388634-T-C

79366667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105388789-T-C

79366667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105388789-T-G

79366715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: synonymous variant
orthologous variants: 105388837-T-G

79368478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105389487-A-G

79369052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105390044-T-A

79369052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105390044-T-C

http://identifiers.org/hco/13/GRCh38#79370859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105390743-A-C

79370859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105390743-A-G

79370997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 105390903-C-T

79371084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 105390990-G-A

79371178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105391080-A-G

http://identifiers.org/hco/13/GRCh38#79371293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105391175-C-A

79371293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105391175-C-G

79371558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105391426-G-A

79371571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105391447-A-T

79371790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392260-A-G

79371790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392260-A-T

79372382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392466-T-C

http://identifiers.org/hco/13/GRCh38#79372476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105392574-A-C

79372627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392727-A-G

79372649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392746-G-A

79373928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105392929-G-A

79374127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105393093-T-C

79374532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105393172-A-G

79375545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: 105394092-T-C

http://identifiers.org/hco/13/GRCh38#79375890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105394392-C-A

79376537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395057-T-C

79376546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395066-T-A

79376640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395155-T-A

79376640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395155-T-C

79376728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395241-A-G

79376890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105395358-T-A

79377107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397010-C-G

79377163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397066-T-C

http://identifiers.org/hco/13/GRCh38#79377212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105397110-C-A

79377212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397110-C-G

79377212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397110-C-T

79377239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397137-T-A

79377239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105397137-T-C

79377372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 105397267-T-C

79377392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105397287-A-G

http://identifiers.org/hco/13/GRCh38#79377412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105397307-A-C

79377432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105397327-T-C

79377441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105397336-A-G

79377472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105397367-T-C

79377472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105397367-T-G

79378898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105398040-T-C

79378914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105398056-A-G

79384130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105400928-G-C

79384684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105401234-T-C

79385058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105401594-T-A

79385135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105401670-T-C

79385150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105401684-A-G

79398510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105405405-T-C

79401623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105409285-G-C

79401945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105409605-T-C

79401945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105409605-T-G

79402575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105411262-G-A

79402937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105411498-C-T

79403288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105411821-T-C

79403453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105411939-A-G

79403770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412186-C-G

79403878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412402-G-A

79403890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412405-T-C

79403926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412451-T-C

79404056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412540-T-C

79404361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105412848-T-C

79404623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105413099-C-T

79404627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105413103-T-C

79404686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105413158-G-A

79405195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105413666-G-A

http://identifiers.org/hco/13/GRCh38#79405432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105413902-C-A

http://identifiers.org/hco/13/GRCh38#79405514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105414021-C-A

http://identifiers.org/hco/13/GRCh38#79405941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#105414438-A-C

79405941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414438-A-T

79405967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414464-G-A

79405967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414464-G-C

79406005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414504-T-A

79406005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414504-T-C

79406005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414504-T-G

http://identifiers.org/hco/13/GRCh38#79406081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#105414582-C-A

79406081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414582-C-T

79406094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414595-G-A

79406102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105414604-T-C

79406171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414677-G-A

79406171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414677-G-T

http://identifiers.org/hco/13/GRCh38#79406210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#105414715-C-A

79406210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414715-C-G

79406229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414734-T-A

79406229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105414734-T-G

79406259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414765-G-C

79406259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414765-G-T

79406302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414809-G-A

79406302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414809-G-T

79406331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non coding transcript exon variant
orthologous variants: 105414838-T-C

79406331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non coding transcript exon variant
orthologous variants: 105414838-T-G

79406377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414887-T-C

79406398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20327
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 105414905-T-C