60752022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108421343-A-G

60752238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108421166-A-G

60752238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108421166-A-T

60752394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108421002-G-T

60753240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108420483-A-G

60753295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108420450-C-G

60753393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108420352-G-T

60753409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108420334-T-C

60753950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108419849-C-T

http://identifiers.org/hco/5/GRCh38#60753956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108419836-C-A

http://identifiers.org/hco/5/GRCh38#60754086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108419712-C-A

60754323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3 prime UTR variant
orthologous variants: 108419491-G-T

60754646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 108419191-G-A

60754820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 108419017-A-G

60754985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108418867-G-T

60755013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108418838-A-T

60755571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108418459-C-T

60756031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417957-A-G

60756093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417896-A-G

60756142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417746-G-C

60756163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417725-C-T

60756222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417642-G-A

60756406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417439-T-C

60756426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417386-G-A

60756448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108417364-A-G

60756847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416977-C-T

60756927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416911-A-G

60756944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416894-A-T

60756994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416844-T-A

60757114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416718-T-C

60757115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416717-A-G

60757385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416428-G-A

60757385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416428-G-C

60757385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416428-G-T

60757585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 108416169-T-C

60757672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416080-G-A

60757672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108416080-G-T

http://identifiers.org/hco/5/GRCh38#60757911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108415842-C-A

60757911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108415842-C-T

60757950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108415807-A-G

http://identifiers.org/hco/5/GRCh38#60758070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108415678-A-C

60758070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108415678-A-T

http://identifiers.org/hco/5/GRCh38#60758424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108415294-A-C

60758475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108415227-T-G

60758557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108415135-T-C

http://identifiers.org/hco/5/GRCh38#60758664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108415055-C-A

60758837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108414956-T-C

60759085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108414601-A-G

60759294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108414426-G-A

60759294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108414426-G-T

60759437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108414267-T-C

60760866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413877-G-C

http://identifiers.org/hco/5/GRCh38#60761118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108413624-A-C

60761121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413621-C-T

60761136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413603-T-A

60761216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413503-G-C

60761328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413391-G-T

http://identifiers.org/hco/5/GRCh38#60761364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108413356-A-C

60762158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413053-G-A

60762158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413053-G-C

60762210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108413002-T-G

60762409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108412923-T-C

60762737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108412358-T-C

60762788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108412325-T-C

60762790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108412323-T-C

60762973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108412168-A-T

60764060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108411085-A-T

60764177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410978-C-T

60764191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410959-G-A

http://identifiers.org/hco/5/GRCh38#60764208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108410942-C-A

60764208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410942-C-G

60764208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410942-C-T

60764277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 108410873-T-C

60764352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410798-A-T

60764402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410751-A-G

http://identifiers.org/hco/5/GRCh38#60764429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108410729-C-A

60764514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410650-G-A

60764614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410545-T-C

60764656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410477-T-C

60764960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410167-T-A

60764960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410167-T-C

60764961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410166-A-G

60764973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108410154-A-G

60765335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108409835-C-T

60765543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108409633-T-C

60765612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108409560-G-C

60765612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108409560-G-T

60766338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408588-G-A

60766338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408588-G-T

60766470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408470-A-G

60766681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408280-T-C

60766694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408175-T-A

60766694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408175-T-G

60766707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408128-T-C

60766707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108408128-T-G

60766754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407966-A-G

60766757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407963-T-A

60766757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407963-T-C

60766846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407876-A-G

60766966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407756-G-C

60767452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407574-T-A

60767801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407267-G-A

60767854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 108407214-A-G

60767896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 108407172-A-T

60767924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407145-A-G

60768022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108407081-G-T

60768533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108406590-G-A

60768533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108406590-G-T

60768731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108406407-C-T

60768733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108406405-T-C

60768909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108406218-T-C

60769067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108405957-T-C

60769184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108405865-T-C

60769615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108405216-T-C

60770148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108405022-T-C

60770196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404973-C-G

60770196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404973-C-T

60770361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404808-C-T

60770401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404769-A-G

60770524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404679-A-G

http://identifiers.org/hco/5/GRCh38#60770525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108404678-C-A

60771378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404358-G-T

http://identifiers.org/hco/5/GRCh38#60771758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108404054-C-A

60771758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404054-C-T

60771771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404041-T-A

60771797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404025-T-A

60771797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404025-T-C

60771806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108404016-A-T

http://identifiers.org/hco/5/GRCh38#60771863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108403953-C-A

60771863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108403953-C-T

60771927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108403888-G-A

60771927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108403888-G-C

60771927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108403888-G-T

60772171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108403657-A-G

60772221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108403624-G-A

60773439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401908-A-G

http://identifiers.org/hco/5/GRCh38#60773549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108401784-C-A

60773549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401784-C-T

60773830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401598-T-C

60776928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401241-C-T

60777507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401073-C-T

60777511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401069-C-G

60777511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108401069-C-T

60777825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400763-C-T

60777837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400752-A-G

60777855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400734-A-G

60777891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400701-A-G

60778063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400333-A-G

http://identifiers.org/hco/5/GRCh38#60778098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108400297-C-A

http://identifiers.org/hco/5/GRCh38#60778143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108400253-C-A

60778156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108400240-T-C

60781311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108399924-T-A

60781311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108399924-T-C

60781416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108399819-T-G

60781486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108399745-G-T

60781568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108399663-T-A

60781987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108398904-A-T

60782065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108398824-T-C

60782065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108398824-T-G

http://identifiers.org/hco/5/GRCh38#60782748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108398071-A-C

60782772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108398047-G-T

60782824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108398007-G-T

60782871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397964-T-C

http://identifiers.org/hco/5/GRCh38#60783136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108397651-A-C

60783360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397474-T-C

60783489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397346-G-A

60783760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394751-T-C

60783768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394743-C-T

60783950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397125-T-C

60783950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397125-T-G

60784002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397073-G-T

60784052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397023-T-C

60784070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108397001-T-C

60784081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396990-G-C

60784081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396990-G-T

60784088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396983-A-G

60784091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396980-T-C

60784107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108396960-G-A

60784107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108396960-G-T

http://identifiers.org/hco/5/GRCh38#60784110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108396957-C-A

60784110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108396957-C-G

60784110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108396957-C-T

60784144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396928-T-C

60784157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396915-G-A

60784157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396915-G-C

60784157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396915-G-T

60784172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396903-A-G

60784188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396884-T-C

http://identifiers.org/hco/5/GRCh38#60784191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108396881-A-C

60784191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396881-A-G

60784191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108396881-A-T

http://identifiers.org/hco/5/GRCh38#60784210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108396862-A-C

http://identifiers.org/hco/5/GRCh38#60784226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108396846-C-A

60784250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396822-T-C

http://identifiers.org/hco/5/GRCh38#60784281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108396788-C-A

60784419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396198-T-C

60784541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108396078-T-A

60784679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395943-G-A

60784785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395861-C-G

60784814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395833-A-G

60784849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395798-G-C

60784955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395685-G-C

60784981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395662-T-G

60785379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395208-T-C

60785489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108395121-G-A

60785589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394837-G-C

60785673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394751-T-C

60785694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394730-C-T

60785873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108394576-T-G

60785878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108394571-T-C

60786020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108394467-T-C

60786021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108394466-T-C

60786087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394402-A-G

http://identifiers.org/hco/5/GRCh38#60786155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108394342-C-A

60786207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108394233-T-C

60786948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108393694-G-A

http://identifiers.org/hco/5/GRCh38#60787195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108393441-C-A

60787195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108393441-C-T

60787211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108393425-A-G

60787261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108393375-G-A

60787261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108393375-G-T

http://identifiers.org/hco/5/GRCh38#60787401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108393263-C-A

60787401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 108393263-C-T

60787412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 108393252-A-G

60787413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 108393251-C-T

60787452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108393212-A-G

60787452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108393212-A-T

http://identifiers.org/hco/5/GRCh38#60787510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108393154-A-C

http://identifiers.org/hco/5/GRCh38#60787545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108393122-C-A

60802442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388921-G-C

60802518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388852-C-T

60802690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388698-T-C

60802726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388662-A-G

60802777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388606-C-T

60802799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388577-T-G

60803076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388195-T-C

60803122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108388147-A-G

60803245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387992-C-G

60803245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387992-C-T

60803433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387783-T-C

60803584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387609-T-G

http://identifiers.org/hco/5/GRCh38#60803586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108387607-C-A

60803792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387428-T-G

60803904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387333-A-T

60803962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387276-T-C

http://identifiers.org/hco/5/GRCh38#60804005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108387233-A-C

60804005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387233-A-G

60804186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108387068-G-A

60804490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386806-G-A

60804503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386794-G-A

60804676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386628-G-A

60804698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386606-T-C

60804882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386425-T-G

60805008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386307-T-C

60805170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386143-C-T

60805195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386118-G-A

60805284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108386019-T-A

http://identifiers.org/hco/5/GRCh38#60805439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108385870-C-A

60805466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108385843-G-A

60805820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108385522-T-C

60805906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108385439-T-G

60805907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108385438-G-A

60806235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384920-C-G

60806282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384873-T-C

60806401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384732-G-A

60806411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384722-G-A

60806421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384712-C-T

60806605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384534-G-A

60806605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384534-G-T

60806607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384532-T-A

60806607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384532-T-C

60806852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384579-G-A

http://identifiers.org/hco/5/GRCh38#60806903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108384541-A-C

60806903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108384541-A-T

60809379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108382326-G-T

60809391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108382314-T-C

60809528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108382187-G-A

60810263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108381131-A-T

60810722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 108380256-A-G

60810917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 108380053-G-A

60810917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 108380053-G-C

60810998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 108379979-A-T

60811059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108379918-T-C

60812892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378350-C-T

60812898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378344-A-G

http://identifiers.org/hco/5/GRCh38#60812910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108378332-A-C

60812927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378279-A-G

60812928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378278-T-A

60812945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378240-G-C

60812956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378210-A-G

60813004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108378113-C-G

60813224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108377946-C-T

60813316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108377844-G-A

60813722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108377113-A-G

60813771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376972-G-C

60813771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376972-G-T

60813832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376914-A-G

60813884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376858-C-G

60813915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376828-C-T

60813932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376813-T-C

60814090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376654-C-T

60814144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376601-T-C

60814283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376436-C-G

60814530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376230-C-T

60814612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376148-T-C

60814632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108376128-T-A

60814921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371926-C-T

60815008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371843-C-T

60815048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371806-T-G

60815050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371804-T-C

60815252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371593-T-C

60815858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371249-T-C

60815958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371149-C-T

60815995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108371122-C-G

60816528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108370952-C-T

60818337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108369053-A-T

60818370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108369023-T-A

60818648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368730-A-G

60818656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368722-C-T

60818801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368581-T-A

60819008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368500-G-C

60819008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368500-G-T

60819014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368494-A-G

http://identifiers.org/hco/5/GRCh38#60819161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108368472-A-C

60819161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368472-A-T

http://identifiers.org/hco/5/GRCh38#60819173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108368460-A-C

60819173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108368460-A-T

60819890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108367702-T-C

60820511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366971-T-C

60820616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366911-C-G

60820616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366911-C-T

60820732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366809-T-C

60820778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366762-G-T

60821117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366629-C-T

http://identifiers.org/hco/5/GRCh38#60821131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#108366615-C-A

60821472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108366281-A-G

60821925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108365886-C-T

60822042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108365762-A-G

60822064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108365740-A-G

60822075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108365729-C-T

60822117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108365695-G-A

60822662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364979-G-A

60822662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364979-G-C

http://identifiers.org/hco/5/GRCh38#60822699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108364942-A-C

http://identifiers.org/hco/5/GRCh38#60822760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108364882-C-A

60822760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364882-C-T

60822871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364797-G-C

60823360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364290-G-A

60823572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364130-T-C

60823597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108364092-T-A

60824014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108363334-A-G

60824090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108363273-C-T

60824427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362951-G-A

60824442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362942-G-A

60824644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362727-A-G

60827464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362572-A-G

60827554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362478-G-T

60827621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362430-A-T

http://identifiers.org/hco/5/GRCh38#60827680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108362371-C-A

60827680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362371-C-T

60827712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362330-T-A

60827831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362230-T-C

60827865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108362186-T-C

60829799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108360557-A-G

60829854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108360503-T-G

http://identifiers.org/hco/5/GRCh38#60829921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108360434-A-C

60830134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359919-G-C

60830247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359805-T-G

60830303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359746-T-C

60830488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359535-G-C

60830631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359419-A-T

60830632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359418-T-A

60830632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359418-T-C

60830632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359418-T-G

60830639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359417-T-C

60830698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108359366-A-T

60833816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108358881-A-G

60836299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356686-G-A

http://identifiers.org/hco/5/GRCh38#60836309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108356676-A-C

60836407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356582-A-T

60836491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356492-G-A

60836864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356175-T-A

60836962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356095-G-A

60836962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108356095-G-C

60837586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108355831-G-A

60837586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108355831-G-C

60838052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108355688-G-A

60838186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108355547-G-A

60838694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108354717-G-A

60838694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108354717-G-C

http://identifiers.org/hco/5/GRCh38#60841526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108353596-C-A

60841549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108353573-T-A

60841603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108353532-G-T

http://identifiers.org/hco/5/GRCh38#60841722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108353413-C-A

60841990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108353153-A-T

60842218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108352660-G-A

60842456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108352418-T-G

60842665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108352151-T-C

60842693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108352120-C-T

60843001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351931-T-C

60843019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351914-G-A

60843277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351680-G-A

60843324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351635-T-C

60843416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351586-C-T

60843417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 108351585-G-A

60843442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351573-G-C

60843543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351474-A-G

60843543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351474-A-T

http://identifiers.org/hco/5/GRCh38#60843668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108351369-C-A

60843668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351369-C-G

60843668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351369-C-T

http://identifiers.org/hco/5/GRCh38#60843673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108351364-C-A

60843673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 108351364-C-T

60843839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351256-G-C

60843932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351198-G-A

http://identifiers.org/hco/5/GRCh38#60844034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108351136-C-A

60844034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 108351136-C-T

http://identifiers.org/hco/5/GRCh38#60844074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108351118-C-A

60844074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 108351118-C-T

60844216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108350985-G-A

60844216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26292
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108350985-G-T