http://identifiers.org/hco/4/GRCh38#8269804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836759-C-A

8269804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35836759-C-G

8269804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35836759-C-T

http://identifiers.org/hco/4/GRCh38#8269960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836697-C-A

8269960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35836697-C-T

http://identifiers.org/hco/4/GRCh38#8269965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836692-C-A

8269965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35836692-C-G

8269965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35836692-C-T

http://identifiers.org/hco/4/GRCh38#8270004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836635-C-A

8270004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 35836635-C-G

8270004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 35836635-C-T

http://identifiers.org/hco/4/GRCh38#8270101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836538-C-A

8270101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 35836538-C-T

8270131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, undefined
orthologous variants: 35836508-G-A

8270131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, undefined
orthologous variants: 35836508-G-T

8270230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35836409-G-A

8270230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35836409-G-C

8270269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35836370-T-C

8270337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: synonymous variant
orthologous variants: 35836302-G-A

8270337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35836302-G-T

http://identifiers.org/hco/4/GRCh38#8270437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35836225-C-A

8270437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35836225-C-T

8272393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35835541-G-A

http://identifiers.org/hco/4/GRCh38#8272424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35835514-C-A

http://identifiers.org/hco/4/GRCh38#8272589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35835381-A-C

8272807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35835213-A-T

8272880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35835127-C-T

8274111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35834144-G-A

8274111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35834144-G-T

8274131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35834124-C-T

8274305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35833911-G-T

8274834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: 35833491-G-T

http://identifiers.org/hco/4/GRCh38#8275004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35833352-A-C

8276643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35831507-C-T

http://identifiers.org/hco/4/GRCh38#8276887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35831716-A-C

8276989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35831797-C-T

8278130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830989-A-G

8278271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830867-C-T

8278272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830866-G-A

http://identifiers.org/hco/4/GRCh38#8278303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35830841-C-A

8278316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830835-G-A

http://identifiers.org/hco/4/GRCh38#8278349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35830805-C-A

8278349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830805-C-G

8278349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830805-C-T

8278812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35830445-T-C

8281519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35829298-G-A

8281777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35829071-C-G

8281777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35829071-C-T

8281873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828976-T-C

http://identifiers.org/hco/4/GRCh38#8281929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828921-A-C

8282118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828772-G-A

8282179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828713-A-G

8282248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828642-A-G

8282277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828612-G-A

http://identifiers.org/hco/4/GRCh38#8282286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828605-C-A

8282286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828605-C-T

8282400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828510-A-T

8282502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35828408-G-A

8282502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35828408-G-T

8282511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35828399-G-A

http://identifiers.org/hco/4/GRCh38#8282548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828362-C-A

8282548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828362-C-T

8282557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828353-C-T

http://identifiers.org/hco/4/GRCh38#8282558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828352-C-A

8282558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828352-C-T

8282564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828346-G-A

8282564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828346-G-T

http://identifiers.org/hco/4/GRCh38#8282565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828345-C-A

8282565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828345-C-T

http://identifiers.org/hco/4/GRCh38#8282569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828341-C-A

8282569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828341-C-T

http://identifiers.org/hco/4/GRCh38#8282598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35828291-C-A

8282650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828239-G-A

8282650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828239-G-T

8282654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35828235-T-C

8284286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35827094-G-A

8284450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826951-T-C

8284772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826732-C-T

8284800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826704-T-C

8284800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826704-T-G

8284809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826695-G-A

8286295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35826000-C-G

8286316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35825979-C-T

8286385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35825912-G-A

8286431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35825851-G-T

http://identifiers.org/hco/4/GRCh38#8286458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35825819-C-A

8286510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35825781-C-T

8286667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825641-G-A

8286688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825620-C-G

8286694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825614-G-A

8286694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825614-G-T

8286757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825551-A-G

8286757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35825551-A-T

8291087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823793-T-C

8291116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823776-T-C

http://identifiers.org/hco/4/GRCh38#8291277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823658-C-A

8291277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823658-C-T

8291299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823636-T-A

8291299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823636-T-C

http://identifiers.org/hco/4/GRCh38#8291336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823618-C-A

8291336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823618-C-T

8291342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823609-C-T

8291350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823605-C-G

8291350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823605-C-T

8291388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35823568-T-A

8291550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35823406-G-T

8291616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823366-T-A

8291616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823366-T-C

http://identifiers.org/hco/4/GRCh38#8291632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823358-C-A

8291632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823358-C-T

8291633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823357-T-A

8291633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823357-T-C

8291633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823357-T-G

http://identifiers.org/hco/4/GRCh38#8291667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823335-C-A

8291667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823335-C-G

8291667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823335-C-T

http://identifiers.org/hco/4/GRCh38#8291696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823307-A-C

8291715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823286-G-A

8291715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823286-G-T

http://identifiers.org/hco/4/GRCh38#8291835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35823197-C-A

8292010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823051-C-G

8292010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823051-C-T

8292076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823003-G-A

8292076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35823003-G-C

http://identifiers.org/hco/4/GRCh38#8292110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35822964-A-C

8292176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822916-G-A

8292203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822904-G-T

http://identifiers.org/hco/4/GRCh38#8292281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35822829-C-A

8292281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822829-C-T

8292321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 35822788-T-G

8292408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822704-G-A

8292495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822622-G-A

8292495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822622-G-T

8292560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822571-G-T

8292611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822532-G-A

8292677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822465-A-G

8292819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822327-G-A

8292819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822327-G-T

http://identifiers.org/hco/4/GRCh38#8292903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35822301-A-C

8293062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822168-G-T

8293154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822097-T-C

8293155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822096-G-A

8293227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35822045-G-A

http://identifiers.org/hco/4/GRCh38#8293632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35821812-C-A

8293706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821750-A-G

http://identifiers.org/hco/4/GRCh38#8293847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35821648-C-A

8293915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821573-G-T

8293927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821561-G-A

http://identifiers.org/hco/4/GRCh38#8293982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35821524-C-A

8293982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821524-C-T

8294012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821491-G-A

8294012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821491-G-T

8294035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821472-G-T

8294049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821458-T-C

8294087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 35821419-G-C

8294087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 35821419-G-T

8294221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821285-G-A

8294221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821285-G-T

8294324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821192-G-A

8294325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821191-G-A

8294325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821191-G-C

http://identifiers.org/hco/4/GRCh38#8294332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35821185-C-A

8294332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821185-C-T

8294334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821183-T-C

http://identifiers.org/hco/4/GRCh38#8294391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35821130-A-C

8294409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821111-A-G

8294485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35821058-G-A

http://identifiers.org/hco/4/GRCh38#8294618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35820909-A-C

8294618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820909-A-G

8294618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820909-A-T

http://identifiers.org/hco/4/GRCh38#8294636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35820891-C-A

8294636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820891-C-G

8294636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820891-C-T

8294646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820865-A-G

8294653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820846-C-T

8294685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820790-C-T

8294735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820735-C-G

8294749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820721-T-C

8294757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820713-T-C

8294765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820705-T-A

8294768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820702-A-T

8294780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820690-A-G

8294787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820683-C-T

8294788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820682-A-G

8294795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820675-T-A

8294795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820675-T-C

8294805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820662-C-T

http://identifiers.org/hco/4/GRCh38#8294820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35820647-A-C

8294820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820647-A-G

8294829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820638-T-A

8294841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820626-T-C

8294845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820622-C-T

8294848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820619-A-G

8294848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35820619-A-T

http://identifiers.org/hco/4/GRCh38#8294921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35820528-C-A

8295309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819951-G-A

8295430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819834-G-T

8295600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819706-T-C

8295619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819687-G-A

8295619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819687-G-C

8295619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35819687-G-T

8295975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819358-G-T

8296011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819326-C-T

8296012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819325-C-T

8296110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819260-G-A

8296118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819257-G-A

8296118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819257-G-T

http://identifiers.org/hco/4/GRCh38#8296140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35819236-C-A

8296145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819231-C-T

8296148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819228-T-C

8296150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819227-A-G

8296153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819224-T-C

http://identifiers.org/hco/4/GRCh38#8296177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35819200-A-C

8296177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819200-A-G

8296206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819171-T-C

8296368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35819002-G-A

8296553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35818828-G-A

8296553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35818828-G-T

8302541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812874-T-C

8302619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812807-G-T

http://identifiers.org/hco/4/GRCh38#8302635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35812791-C-A

8302635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812791-C-T

http://identifiers.org/hco/4/GRCh38#8303292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35812268-C-A

8303292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812268-C-T

8303426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812076-G-T

8303427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35812075-G-A

8303513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35811994-G-A

8303842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35811788-A-G

8304166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35811528-A-T

8304195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35811497-A-G

http://identifiers.org/hco/4/GRCh38#8304343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35811335-C-A

8304343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: 35811335-C-T

http://identifiers.org/hco/4/GRCh38#8304344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35811334-C-A

8304344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: 35811334-C-G

8304370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35811308-T-A

8304370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35811308-T-G

8305857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: 35810558-T-A

8305871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35810544-A-G

http://identifiers.org/hco/4/GRCh38#8305890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810525-C-A

8305890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron_variant, undefined
orthologous variants: 35810525-C-T

8305898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35810517-C-T

http://identifiers.org/hco/4/GRCh38#8305937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810499-C-A

8305937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35810499-C-G

8305937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: intron variant
orthologous variants: 35810499-C-T

8305987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, undefined
orthologous variants: 35810448-G-C

8305987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense_variant, undefined
orthologous variants: 35810448-G-T

8306056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35810379-A-G

8306056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35810379-A-T

8306083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: missense variant
orthologous variants: 35810352-C-T

8306279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35810160-G-T

http://identifiers.org/hco/4/GRCh38#8306323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810125-C-A

http://identifiers.org/hco/4/GRCh38#8306352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810096-A-C

8306352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35810096-A-G

http://identifiers.org/hco/4/GRCh38#8306356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810092-C-A

http://identifiers.org/hco/4/GRCh38#8306396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35810052-C-A

http://identifiers.org/hco/4/GRCh38#8306448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35809986-C-A

8306448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809986-C-T

8306493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809947-T-C

8306493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809947-T-G

http://identifiers.org/hco/4/GRCh38#8306685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35809758-C-A

http://identifiers.org/hco/4/GRCh38#8306708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35809743-C-A

8306708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809743-C-T

8306774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35809688-G-A

8306774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35809688-G-T

8306794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35809676-T-C

8306858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809616-G-T

8306926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30406
most severe consequence: 3 prime UTR variant
orthologous variants: 35809552-G-A