http://identifiers.org/hco/9/GRCh38#131373657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32028181-C-A

131373657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028181-C-T

131373663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028187-G-A

131373675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028199-T-C

http://identifiers.org/hco/9/GRCh38#131373704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32028228-C-A

131373704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028228-C-T

131373706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028230-G-A

131373706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028230-G-T

131373708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32028232-A-G

131374491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32028688-A-G

131392933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32039086-G-A

131392933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32039086-G-C

131393082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32039169-G-T

131393458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32039757-C-T

131393707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32040750-C-T

131393720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32040766-G-A

131393720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32040766-G-C

131393968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32041006-G-T

131393977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32041015-G-T

131394119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32041154-G-A

131394119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32041154-G-T

131394283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32041323-G-A

http://identifiers.org/hco/9/GRCh38#131394287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32041327-C-A

131394702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32041546-C-T

131394746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32041580-G-A

131394746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32041580-G-C

http://identifiers.org/hco/9/GRCh38#131395041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32041793-A-C

131395503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042267-T-C

131395713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042403-T-C

131395797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042484-T-G

131395832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042542-A-G

http://identifiers.org/hco/9/GRCh38#131395867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32042604-A-C

131395886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042622-C-G

131396078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042800-T-A

131396222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042933-C-T

131396694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32042999-T-A

131396790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043061-C-T

http://identifiers.org/hco/9/GRCh38#131397188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32043415-C-A

131397274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043446-C-G

131397285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043461-G-A

131397285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043461-G-C

http://identifiers.org/hco/9/GRCh38#131397327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32043494-A-C

131397327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043494-A-T

131397427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32043594-A-G

131397444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32043609-G-T

131397548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043691-A-T

131397580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043715-T-G

131397622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32043755-G-T

http://identifiers.org/hco/9/GRCh38#131397658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32043785-C-A

131397889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32044043-T-C

131398001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32044217-C-G

131398234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32044532-G-A

131400498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32045261-A-T

131400573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32045354-C-T

131400598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32045378-G-A

131402630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32047184-G-A

131402713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32047257-T-A

http://identifiers.org/hco/9/GRCh38#131403152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32047593-A-C

131403223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32047657-G-A

http://identifiers.org/hco/9/GRCh38#131404257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32048329-C-A

131404257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32048329-C-T

131405106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32048953-T-C

131405210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32049047-A-G

131405347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32049148-A-G

131405378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32049170-T-A

131406270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050043-A-G

131406282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050057-A-G

131406288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050063-G-A

131406296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050071-G-C

131406304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050079-C-T

http://identifiers.org/hco/9/GRCh38#131406306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32050081-C-A

131406306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050081-C-G

131406316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050091-C-T

131406911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050605-G-A

131406938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32050625-A-G

131415339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32056130-T-A

131418582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32058013-C-G

131418611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32058042-G-A

131419746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32060245-G-A

131420141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32060544-T-G

131420184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32060580-C-T

131420397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32060872-C-T

131420422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32060900-C-T

131422726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32064705-C-T

131422813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32064795-T-A

131423151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065083-G-T

131423174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32065106-G-T

131423305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32065223-G-C

131423305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, undefined
orthologous variants: 32065223-G-T

131423485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065405-A-G

131424546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065895-C-T

131424555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065904-G-A

131424578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065926-C-G

131424578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065926-C-T

131424595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065943-A-T

131424596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065944-G-C

131424625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32065964-A-G

131429851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072279-G-C

http://identifiers.org/hco/9/GRCh38#131429985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32072402-C-A

131429985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072402-C-T

131430052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072440-T-C

131430052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072440-T-G

131430061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072449-T-A

131430061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072449-T-C

131432294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072883-C-G

http://identifiers.org/hco/9/GRCh38#131432333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32072918-C-A

131432333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072918-C-G

131432354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32072938-C-T

131432572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32073096-G-A

131432572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32073096-G-C

http://identifiers.org/hco/9/GRCh38#131432865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32073382-C-A

131432865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32073382-C-T

131436605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32075342-C-T

http://identifiers.org/hco/9/GRCh38#131436738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32075474-C-A

131438374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32076866-G-C

131438586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077076-T-G

131438711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077252-T-A

131438711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077252-T-C

131438719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077260-T-G

131438839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077378-G-T

http://identifiers.org/hco/9/GRCh38#131438848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32077386-C-A

131438848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077386-C-T

http://identifiers.org/hco/9/GRCh38#131438876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32077415-C-A

131438876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077415-C-T

131438877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077416-G-A

131438877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077416-G-C

131438877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077416-G-T

131439074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077578-G-A

131439074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077578-G-C

http://identifiers.org/hco/9/GRCh38#131439096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32077598-C-A

131439139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077627-G-A

131439139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32077627-G-C

131443145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080509-T-A

131443152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080516-G-T

131443240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080591-T-C

131443278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080628-C-T

131443283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080633-G-A

131443353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080693-G-A

131443445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080804-A-T

131443602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32080955-G-A

131443775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081094-G-T

131443882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081207-G-A

131444002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081307-G-C

131444087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081435-C-G

131444087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081435-C-T

131444134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081470-G-A

131444134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081470-G-T

131444143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081479-C-T

131444345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081686-T-C

http://identifiers.org/hco/9/GRCh38#131444396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32081726-C-A

131444396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081726-C-T

131444428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081764-G-A

131444428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081764-G-T

http://identifiers.org/hco/9/GRCh38#131444460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32081799-C-A

131444460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081799-C-T

131444479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081817-A-G

131444479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32081817-A-T

131446053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32083479-T-A

131446195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32083609-G-A

http://identifiers.org/hco/9/GRCh38#131446292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32083680-C-A

131446292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32083680-C-T

http://identifiers.org/hco/9/GRCh38#131446337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32083739-C-A

131446489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32083863-C-T

131446494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32083868-G-A

131446518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32083892-C-T

131446588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32083962-G-A

131446654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084028-G-T

http://identifiers.org/hco/9/GRCh38#131446789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32084145-C-A

131446789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084145-C-T

131446884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084222-T-C

http://identifiers.org/hco/9/GRCh38#131446977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32084288-C-A

131446977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084288-C-G

131446977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084288-C-T

131446980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084291-G-C

http://identifiers.org/hco/9/GRCh38#131446992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32084305-C-A

131446992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084305-C-T

131446993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084306-A-G

131447067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084374-A-G

131447116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32084423-G-A

131447138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32084445-T-C

131447270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084562-G-A

131447270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084562-G-C

131447272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084564-G-C

131447272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084564-G-T

131447351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084593-T-C

131447351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084593-T-G

131447531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084752-T-G

131447534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084754-A-T

131447588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084799-T-A

131447622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084826-T-A

131447622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084826-T-C

131447624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084828-T-C

131447689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32084893-C-T

131447729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32084933-C-T

131447797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32085001-C-G

131455262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32089222-T-C

131459034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32090707-G-A

http://identifiers.org/hco/9/GRCh38#131459101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32090783-C-A

http://identifiers.org/hco/9/GRCh38#131459114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32090796-A-C

131459114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32090796-A-G

131459169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32090843-G-A

131459169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32090843-G-C

131459169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32090843-G-T

131459194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32090868-G-A

http://identifiers.org/hco/9/GRCh38#131459263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32090937-A-C

131459263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32090937-A-G

131459285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32090959-G-A

131464756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32094014-T-G

http://identifiers.org/hco/9/GRCh38#131464968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32094226-A-C

http://identifiers.org/hco/9/GRCh38#131465062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32094320-C-A

131465062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32094320-C-T

131465073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32094331-A-G

131465073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32094331-A-T

131465081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32094339-A-G

131467399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096197-G-A

131467464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096256-G-A

131467464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096256-G-T

131467489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096278-C-T

131467738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32096553-G-C

http://identifiers.org/hco/9/GRCh38#131467805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32096619-C-A

http://identifiers.org/hco/9/GRCh38#131467857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32096638-C-A

131467857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096638-C-T

http://identifiers.org/hco/9/GRCh38#131467866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32096647-C-A

131467866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096647-C-T

http://identifiers.org/hco/9/GRCh38#131467876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32096657-C-A

131467876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096657-C-T

131467882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096663-G-T

131467986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096733-A-T

131467987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096734-T-A

131468196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096878-C-G

131468305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32096981-G-A

131468501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32097150-G-A

131468536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32097187-C-G

131468958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32097587-G-A

131469961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098047-A-G

131470031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098110-G-A

131470105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098175-G-A

131470134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098194-A-G

131470140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098200-A-G

131470144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098204-G-A

131470144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098204-G-T

131470148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098208-G-A

131470242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098277-G-A

131470242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098277-G-T

131470589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098486-T-C

131470640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098530-A-T

131470747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098618-G-T

http://identifiers.org/hco/9/GRCh38#131470768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32098635-C-A

131470768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098635-C-G

131470768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098635-C-T

http://identifiers.org/hco/9/GRCh38#131470772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32098639-C-A

131470772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098639-C-T

131470810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32098674-A-T

131470922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32098786-C-T

131470949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32098813-G-A

131470949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32098813-G-C

131470993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098857-G-A

131471033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098899-G-A

131471033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098899-G-T

131471045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32098911-T-C

http://identifiers.org/hco/9/GRCh38#131473400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32101981-A-C

131473400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32101981-A-T

131473408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32101988-G-A

131473408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32101988-G-T

131473452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32102030-G-A

http://identifiers.org/hco/9/GRCh38#131473754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32102319-C-A

131473754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32102319-C-T

http://identifiers.org/hco/9/GRCh38#131473755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32102320-C-A

131473755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32102320-C-T

131474007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32102539-G-A

131474007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32102539-G-C

131474767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103212-G-A

131474767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103212-G-T

131474796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103241-G-A

131474847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103292-G-A

131474847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103292-G-C

131474964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103409-A-T

131475183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103619-C-T

http://identifiers.org/hco/9/GRCh38#131475233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32103669-C-A

131475233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103669-C-G

131475233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103669-C-T

131475362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103801-G-A

131475388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103827-G-A

131475388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103827-G-C

131475388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32103827-G-T

131475402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103841-G-T

http://identifiers.org/hco/9/GRCh38#131475423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32103862-C-A

131475423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103862-C-T

131475531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32103970-C-T

131475596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104035-G-C

131475799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104223-T-A

131475799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104223-T-C

131475861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104285-A-G

131475898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104322-C-T

131475937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104361-G-C

131475969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104393-A-G

http://identifiers.org/hco/9/GRCh38#131475990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32104414-C-A

131475990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104414-C-T

131476002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104426-T-C

131476298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104722-G-A

131476310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, missense_variant
orthologous variants: 32104734-G-A

http://identifiers.org/hco/9/GRCh38#131476320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32104744-C-A

131476320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104744-C-T

131476410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32104834-G-A

http://identifiers.org/hco/9/GRCh38#131476652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32105060-C-A

131476652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105060-C-T

131476778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105215-C-T

131476856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105282-G-A

131476856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105282-G-T

131477179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105545-T-G

131477258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105618-A-G

131477258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105618-A-T

131477509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105834-C-T

131477632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105935-T-C

131477634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105937-G-A

131477634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105937-G-C

131477634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32105937-G-T

131477795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32106091-T-G

131477824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32106120-C-T

131477838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32106134-G-T

131477889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32106185-G-T

131478066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106294-G-T

131478200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106379-G-T

131478213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106402-C-T

131478394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106551-C-T

http://identifiers.org/hco/9/GRCh38#131478400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32106568-C-A

131478400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106568-C-T

http://identifiers.org/hco/9/GRCh38#131478749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32106807-A-C

131478749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106807-A-G

131478751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106809-C-T

http://identifiers.org/hco/9/GRCh38#131478759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32106817-C-A

131478998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32106974-G-A

131479047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107019-C-T

131479126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107094-G-A

131479126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107094-G-T

http://identifiers.org/hco/9/GRCh38#131479204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32107155-C-A

131479204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107155-C-T

131479382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32107336-G-A

131479487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107414-A-G

131479532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107449-G-A

131479532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32107449-G-T

131481541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108474-G-A

131481591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108544-C-G

131481591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108544-C-T

131481596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108549-G-A

131481596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108549-G-T

http://identifiers.org/hco/9/GRCh38#131481616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32108561-A-C

131481616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108561-A-T

131481617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108562-G-A

131481617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108562-G-C

131481617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108562-G-T

131481620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108565-G-C

131481620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108565-G-T

131481673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108625-T-C

http://identifiers.org/hco/9/GRCh38#131481700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32108662-C-A

131481700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108662-C-T

http://identifiers.org/hco/9/GRCh38#131481742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32108705-C-A

131481742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32108705-C-T

http://identifiers.org/hco/9/GRCh38#131481743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32108706-C-A

131481743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32108706-C-G

131481743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32108706-C-T

131481745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32108708-A-G

131481918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32108805-C-T

131482187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109042-G-A

131482195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109050-T-C

131482239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109084-A-G

131482242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109089-A-G

131482255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109102-G-T

131482293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109142-C-G

131482293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109142-C-T

131482295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109144-G-A

131482295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109144-G-C

131482295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109144-G-T

http://identifiers.org/hco/9/GRCh38#131482299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32109148-C-A

131482307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109156-G-A

131482327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109175-G-A

131482327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109175-G-T

131482406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109261-T-G

131482433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109288-G-A

131482493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109348-C-T

131482514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109369-C-T

131482553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109408-T-A

131482553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109408-T-G

http://identifiers.org/hco/9/GRCh38#131482766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32109608-C-A

131482766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109608-C-T

131482865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32109707-C-T

131482918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109759-G-T

131482927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109768-T-C

http://identifiers.org/hco/9/GRCh38#131483035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32109854-C-A

131483035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109854-C-T

131483036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109855-G-A

131483036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109855-G-C

131483036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109855-G-T

131483073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32109887-T-C

131483275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110031-A-G

131483286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110036-T-G

131483298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110047-T-C

131483398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32110141-C-G

131483398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32110141-C-T

131483408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32110151-G-T

http://identifiers.org/hco/9/GRCh38#131483412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32110155-A-C

131483448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110191-A-G

http://identifiers.org/hco/9/GRCh38#131483470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32110213-C-A

131483470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110213-C-T

131483804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110474-C-T

131484022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32110647-A-G

http://identifiers.org/hco/9/GRCh38#131484330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32110930-A-C

http://identifiers.org/hco/9/GRCh38#131484642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32111055-C-A

131484823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111230-C-G

131484823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111230-C-T

http://identifiers.org/hco/9/GRCh38#131484863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32111268-C-A

131484865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111270-C-T

131484866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111271-G-A

131484866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111271-G-T

131485157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111566-G-A

131485157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111566-G-T

http://identifiers.org/hco/9/GRCh38#131485178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32111586-C-A

131485178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111586-C-T

131485315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111701-C-G

131485507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111868-G-T

131485586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32111926-T-A

131485748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32112064-A-G

131485947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112187-T-C

131485948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112188-A-G

131486012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112248-G-C

131486012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112248-G-T

http://identifiers.org/hco/9/GRCh38#131486044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112263-C-A

http://identifiers.org/hco/9/GRCh38#131486070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112287-C-A

131486070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112287-C-T

http://identifiers.org/hco/9/GRCh38#131486075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112292-C-A

131486075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112292-C-G

131486189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 32112406-G-A

131486204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112421-G-A

131486204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112421-G-T

http://identifiers.org/hco/9/GRCh38#131486205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112422-C-A

131486205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112422-C-T

http://identifiers.org/hco/9/GRCh38#131486237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112445-A-C

131486237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112445-A-T

http://identifiers.org/hco/9/GRCh38#131486273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112473-C-A

131486273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112473-C-T

131486366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112535-G-T

http://identifiers.org/hco/9/GRCh38#131486583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112720-C-A

131486583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112720-C-T

http://identifiers.org/hco/9/GRCh38#131486628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32112762-C-A

131486628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32112762-C-T

131487031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113317-A-G

131487031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113317-A-T

131487126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113398-G-A

131487126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113398-G-T

131487136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113408-T-C

131487157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113421-C-T

131487539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113666-T-G

131487671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113795-C-T

131487741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113837-G-T

131487778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113863-G-A

131487778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113863-G-C

131487778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32113863-G-T

131487910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: synonymous variant
orthologous variants: 32113995-T-C

131488091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense variant
orthologous variants: 32114176-C-T

131490604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32115783-G-C

131490763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron variant
orthologous variants: 32115917-C-T

http://identifiers.org/hco/9/GRCh38#131490797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32115949-C-A

131490807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32115959-C-T

131490827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32115979-A-G

http://identifiers.org/hco/9/GRCh38#131490845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32115997-C-A

131490845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32115997-C-G

131490845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32115997-C-T

131490852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116001-T-A

131490852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116001-T-C

131490852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116001-T-G

http://identifiers.org/hco/9/GRCh38#131490857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116006-A-C

131490857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116006-A-G

131490928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116032-G-A

131490928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116032-G-T

131491007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116076-G-C

131491034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116103-G-A

131491034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116103-G-T

131491047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32116116-C-T

131491561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32116379-T-C

131491605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116408-A-G

http://identifiers.org/hco/9/GRCh38#131491676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116475-C-A

131491676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116475-C-T

http://identifiers.org/hco/9/GRCh38#131491692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116490-C-A

131491692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116490-C-T

131491700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116498-G-T

131491706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116505-A-G

131491777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116562-A-G

131491795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116583-C-G

131492107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116896-G-A

131492107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116896-G-T

131492108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116897-T-C

http://identifiers.org/hco/9/GRCh38#131492117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116907-C-A

131492117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116907-C-T

131492130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116920-G-A

131492130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116920-G-T

http://identifiers.org/hco/9/GRCh38#131492132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116922-C-A

131492144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116932-G-A

131492144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116932-G-C

131492144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116932-G-T

131492159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32116947-G-A

http://identifiers.org/hco/9/GRCh38#131492192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32116980-C-A

131492441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32117199-G-C

131492741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32117575-C-T

131493749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118734-G-A

131493749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118734-G-C

131493762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118747-C-T

131493764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118751-C-G

131493972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118889-C-G

131493995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118912-G-C

131494093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119022-C-T

131495140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120007-G-T

131495434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120381-G-A

131495517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120458-G-A

131495517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120458-G-T

131495654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120551-G-A

131495654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120551-G-C

131495654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120551-G-T

http://identifiers.org/hco/9/GRCh38#131495666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32120563-A-C

131495666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120563-A-G

http://identifiers.org/hco/9/GRCh38#131495892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32120769-C-A

131495892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120769-C-G

131495892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120769-C-T

131495919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120794-C-T

131495923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120798-A-G

131495923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120798-A-T

http://identifiers.org/hco/9/GRCh38#131496006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32120869-C-A

131496006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32120869-C-T

http://identifiers.org/hco/9/GRCh38#131496355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32121157-A-C

131496355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121157-A-G

http://identifiers.org/hco/9/GRCh38#131496508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32121344-C-A

131496563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121372-T-G

131496766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121502-G-A

131496766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121502-G-T

131496772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121508-G-A

131496772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121508-G-T

131496912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121599-G-A

131496912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121599-G-T

131497070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121730-T-C

131497250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121900-G-T

131497281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121935-C-G

131497281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121935-C-T

131497284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32121938-G-T

131497381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122031-G-A

http://identifiers.org/hco/9/GRCh38#131497431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122075-C-A

131497458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122111-A-G

131497481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122133-G-A

131497481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122133-G-T

131497637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122245-G-T

131497719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122326-C-T

131497746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122353-G-A

131497746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122353-G-T

131497750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122357-T-C

131497792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122380-A-G

131497874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122460-G-A

http://identifiers.org/hco/9/GRCh38#131497963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122517-C-A

131497963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122517-C-T

131498017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122559-T-C

http://identifiers.org/hco/9/GRCh38#131498083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122654-C-A

131498148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122716-G-A

131498156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122724-G-A

131498176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122742-T-C

http://identifiers.org/hco/9/GRCh38#131498178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122744-C-A

http://identifiers.org/hco/9/GRCh38#131498179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122745-C-A

131498179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32122745-C-T

http://identifiers.org/hco/9/GRCh38#131498211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32122772-C-A

http://identifiers.org/hco/9/GRCh38#131498470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32123023-C-A

131498470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123023-C-T

131498668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123216-A-G

131498742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123287-C-G

131498751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123296-G-A

131498751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123296-G-T

131498905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123411-C-T

131498946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123449-T-G

131499110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123600-G-A

131499110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123600-G-T

131499173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123641-C-T

131499231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123692-T-C

131499266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123733-G-A

131499266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123733-G-C

131499266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123733-G-T

131499343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123806-A-G

http://identifiers.org/hco/9/GRCh38#131499516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32123945-C-A

131499534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123957-G-A

131499534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123957-G-T

131499555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123981-A-G

131499571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32123995-A-G

http://identifiers.org/hco/9/GRCh38#131499682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32124090-C-A

131499884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32124256-T-A

131499884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32124256-T-C

131499933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32124295-T-C

http://identifiers.org/hco/9/GRCh38#131499949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32124310-C-A

131499984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32124344-G-T

131500103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28121
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32124435-A-T