99262968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5 prime UTR variant
orthologous variants: 117155290-T-C

99262968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5 prime UTR variant
orthologous variants: 117155290-T-G

http://identifiers.org/hco/1/GRCh38#99263445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117154862-C-A

99263540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154767-G-A

99263671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154647-T-G

99263787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154538-G-A

99263846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154492-G-T

http://identifiers.org/hco/1/GRCh38#99263869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117154467-C-A

99263869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154467-C-T

99263997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154357-C-T

99264071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154286-C-T

http://identifiers.org/hco/1/GRCh38#99264082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117154276-A-C

99264082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154276-A-G

99264136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154228-A-G

99264171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117154182-T-C

99264252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117154093-G-A

99264252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117154093-G-C

99264252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117154093-G-T

http://identifiers.org/hco/1/GRCh38#99264406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#117153939-C-A

99264406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117153939-C-G

http://identifiers.org/hco/1/GRCh38#99264570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#117153772-C-A

99264570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117153772-C-T

99264710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153631-T-C

99264741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153600-A-G

http://identifiers.org/hco/1/GRCh38#99264754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117153583-C-A

99264754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153583-C-T

99264755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153582-G-A

99264755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153582-G-C

99264755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153582-G-T

99264775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117153564-G-A

99264775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117153564-G-C

99264775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117153564-G-T

99264863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117153467-C-T

99264883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153447-G-A

99265046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153293-G-A

http://identifiers.org/hco/1/GRCh38#99265151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117153180-C-A

99265151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153180-C-G

99265284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117153030-G-A

99265689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117152567-G-A

99265761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117152496-T-C

99265826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117152429-T-C

99265867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117152388-T-C

99265939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117152316-T-C

99266390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117151856-A-G

99266648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117151610-A-G

http://identifiers.org/hco/1/GRCh38#99266793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117151274-C-A

99266879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, undefined
orthologous variants: 117151189-T-G

99266964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117151102-T-C

http://identifiers.org/hco/1/GRCh38#99266986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117151080-A-C

99267010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117151057-G-C

99267126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117150971-G-A

99267131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117150966-C-T

99267573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117150184-G-A

99268120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117149439-C-T

99268221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117149232-C-T

99268223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117149226-G-A

99268280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117149170-A-G

99268457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117149025-C-T

99268711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117148769-G-A

99268805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117148703-C-T

99268897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117148602-A-G

99270796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117147852-A-G

99270832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117147818-C-G

99270937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117147707-T-A

99271021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117147619-T-C

99271499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146939-G-T

99271503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146935-G-C

99271564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146876-T-C

99271682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146749-C-T

99271777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146660-A-G

99271938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146538-G-C

99271958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146518-C-G

99271964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146512-G-A

99272039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146450-T-A

http://identifiers.org/hco/1/GRCh38#99272180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117146314-A-C

99272293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146214-C-T

http://identifiers.org/hco/1/GRCh38#99272317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117146191-C-A

99272317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146191-C-T

99272341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117146166-A-G

99272670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117144406-C-G

99272846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117144235-A-G

99273014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117143110-T-A

99273050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117143069-T-C

99273050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117143069-T-G

99273072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117143049-G-A

99273190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142920-A-G

99273215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142895-G-C

99273237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142852-G-A

99273277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142816-C-G

99273332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142765-G-A

99273457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142642-T-C

99273585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142532-G-A

99273629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142486-T-C

99273722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142392-A-G

http://identifiers.org/hco/1/GRCh38#99273756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117142358-A-C

99273806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142205-A-G

99273935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142073-T-C

99273998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117142011-C-T

http://identifiers.org/hco/1/GRCh38#99277997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117141885-C-A

99278134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117141763-T-C

99278379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117141569-G-A

http://identifiers.org/hco/1/GRCh38#99278643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117141304-A-C

99279088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117140784-T-C

99279147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117140725-A-G

99279566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117140307-G-A

99279683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117140189-T-C

99279786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117140079-A-G

99280110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139758-C-T

99280218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139697-A-G

99280286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139635-T-C

99280353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139563-A-G

99280405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139511-T-C

99280623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139309-T-C

99280653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139279-T-C

99280654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117139278-T-C

99281002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138953-T-A

99281073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138888-G-A

99281144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138817-T-C

99281207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138753-T-G

99281225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138732-C-T

99281383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138612-A-G

99281584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138433-A-G

99281690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138333-T-A

99281690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117138333-T-C

99281762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137616-T-C

99282009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137380-G-T

99282093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137282-C-G

99282254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137097-C-T

99282255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137096-A-G

99282311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117137047-T-A

99282477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136885-G-A

99282496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136871-A-T

99282574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136788-A-G

99282807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136611-T-C

http://identifiers.org/hco/1/GRCh38#99282890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117136543-C-A

99282890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136543-C-G

99282890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136543-C-T

99283046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136474-G-T

99283151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136369-A-G

99283177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136343-A-G

99283299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136224-G-C

99283394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136129-T-C

99283394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117136129-T-G

99283575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135919-T-C

99284102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135733-T-C

99284210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135628-T-C

99284440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135448-A-G

99284486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135429-A-G

99284755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135301-G-A

99284822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135238-T-C

99284822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135238-T-G

99284856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117135198-T-C

http://identifiers.org/hco/1/GRCh38#99284919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117135153-A-C

http://identifiers.org/hco/1/GRCh38#99285566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117132578-A-C

99285594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117132550-T-C

99285636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117132520-C-T

http://identifiers.org/hco/1/GRCh38#99285691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117132472-C-A

http://identifiers.org/hco/1/GRCh38#99286102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117132201-C-A

99286257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117132052-A-G

99286344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131966-T-C

99286371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131939-A-G

99286371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131939-A-T

99286376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131934-T-C

99286515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131760-T-C

http://identifiers.org/hco/1/GRCh38#99286594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117131689-C-A

99286594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131689-C-T

99286595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131688-G-A

99286634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131649-G-A

http://identifiers.org/hco/1/GRCh38#99286709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117131577-C-A

99286709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117131577-C-T

http://identifiers.org/hco/1/GRCh38#99286717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117131569-A-C

99287830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129385-A-T

99287847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129368-A-G

99287871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129346-G-A

99287871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129346-G-T

99287958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117129245-T-C

99288007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 117129196-G-A

99288031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 117129172-G-A

99288031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 117129172-G-T

99288079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense variant
orthologous variants: 117129124-A-G

http://identifiers.org/hco/1/GRCh38#99288166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117129037-A-C

99288166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129037-A-G

99288166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129037-A-T

99288180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129023-C-T

99288202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117129001-A-G

99288225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128978-T-C

http://identifiers.org/hco/1/GRCh38#99288234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117128958-A-C

99288242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128950-G-A

99288242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128950-G-C

99288276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128907-T-A

99288276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128907-T-C

99288590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117128602-T-C

99289076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117127274-A-G

99289141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117127210-T-A

99295116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117127110-C-T

http://identifiers.org/hco/1/GRCh38#99295250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117126980-A-C

99295271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126960-T-G

99295280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126951-A-G

99295491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126789-C-T

99295616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126734-T-A

99295617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126733-T-G

99295666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126685-G-A

99295768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126603-T-A

http://identifiers.org/hco/1/GRCh38#99295779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117126592-C-A

99295780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126591-A-T

99295872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126509-C-G

99296084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126267-G-T

99296093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126232-G-A

99296152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126165-C-T

99296204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126116-G-C

99296204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126116-G-T

99296263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126060-T-C

99296301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117126025-A-G

99296438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125890-G-A

99296543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125607-T-A

99296591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125560-T-C

99296625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125529-A-G

99296644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125510-G-C

99296644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125510-G-T

99296656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125497-A-G

http://identifiers.org/hco/1/GRCh38#99296670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117125483-C-A

99296670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125483-C-T

99296872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125290-G-A

99296912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125255-T-C

99297064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125099-T-C

99297071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117125092-T-C

99297192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124802-A-G

http://identifiers.org/hco/1/GRCh38#99297200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117124794-C-A

99297200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124794-C-T

99297607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124305-T-C

99297633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124279-C-T

99297689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124220-G-A

99297754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117124152-G-A

99297937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123680-G-C

http://identifiers.org/hco/1/GRCh38#99297942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117123675-A-C

http://identifiers.org/hco/1/GRCh38#99298042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117123483-C-A

99298083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123450-G-A

99298136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123400-A-T

99298152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123384-C-T

99298413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123168-C-G

99298413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123168-C-T

99298433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123148-A-G

99298451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123132-G-A

99298486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123108-C-T

99298571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117123024-A-G

99298612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122981-G-T

99298721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122545-T-A

http://identifiers.org/hco/1/GRCh38#99298731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117122535-A-C

99298731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122535-A-G

http://identifiers.org/hco/1/GRCh38#99298785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117122478-A-C

99298789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122474-T-A

99298789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122474-T-C

99298791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122472-G-T

99298835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122215-T-A

99298835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122215-T-G

99298850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122200-G-A

99298850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron variant
orthologous variants: 117122200-G-T

http://identifiers.org/hco/1/GRCh38#99298948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117122128-A-C

99298967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117122112-T-A

99299273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121793-T-C

99299294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121776-A-G

99299308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121766-G-A

http://identifiers.org/hco/1/GRCh38#99299324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117121750-A-C

99299347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121727-T-A

http://identifiers.org/hco/1/GRCh38#99299379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117121695-A-C

99299544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121579-T-C

http://identifiers.org/hco/1/GRCh38#99299565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117121558-A-C

99299576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121547-C-T

http://identifiers.org/hco/1/GRCh38#99299591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117121532-A-C

99299596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121526-C-G

99299677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121444-G-A

99299678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121443-G-A

http://identifiers.org/hco/1/GRCh38#99299797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117121379-C-A

99299797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121379-C-T

99299943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121231-T-C

99299977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121197-C-G

99300209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117121069-G-A

99300369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120908-A-G

99300527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120764-A-G

99300592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120698-C-T

99300834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120464-A-T

99300919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117120379-C-T

99300975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120323-C-T

http://identifiers.org/hco/1/GRCh38#99301118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117120209-C-A

99301148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120180-A-G

99301252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120071-C-T

99301320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117120026-T-C

99301347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119998-T-C

99301347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119998-T-G

99301482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119862-G-T

99301568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119772-A-G

99301576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119764-T-C

99301588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119752-G-T

99301592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119748-A-G

http://identifiers.org/hco/1/GRCh38#99301597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117119743-C-A

http://identifiers.org/hco/1/GRCh38#99301705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117119629-C-A

99301705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119629-C-T

99302184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117119087-C-T

99302340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118935-G-A

99302349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118924-C-G

http://identifiers.org/hco/1/GRCh38#99302419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117118854-A-C

99303244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118579-G-A

99303335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118488-T-A

99303408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118413-G-A

99303483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118331-A-G

99303493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117118321-C-G

99304031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117117840-C-T

99304057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117117814-C-T

99305579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117116994-T-G

99305657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117116912-A-G

99305844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116725-C-T

99305940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116629-G-A

99305940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116629-G-C

http://identifiers.org/hco/1/GRCh38#99305973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117116596-C-A

99305973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116596-C-G

99305973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 117116596-C-T

99306102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116467-T-A

http://identifiers.org/hco/1/GRCh38#99306208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117116358-C-A

99306388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 117116178-G-A

99306561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117116005-C-T

99306615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117115951-A-G

http://identifiers.org/hco/1/GRCh38#99307206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117115285-A-C

99307217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115274-G-A

99307217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115274-G-C

99307217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115274-G-T

http://identifiers.org/hco/1/GRCh38#99307259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117115249-A-C

99307326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115183-T-C

99307345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115164-G-T

99307409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115093-T-C

http://identifiers.org/hco/1/GRCh38#99307484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117115014-A-C

99307484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117115014-A-G

99307647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117114719-G-A

99308029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117114341-T-C

99308301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117114079-A-G

99308338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117114042-T-A

99308412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113965-T-C

99308548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113822-G-T

99308571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113799-G-A

http://identifiers.org/hco/1/GRCh38#99308597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117113759-C-A

http://identifiers.org/hco/1/GRCh38#99308768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117113588-A-C

http://identifiers.org/hco/1/GRCh38#99308863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#117113493-C-A

99308863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113493-C-T

99308895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113462-G-A

99308895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113462-G-C

99308953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113422-A-G

99308961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113414-A-G

99308970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113405-A-G

99309151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117113223-A-G