72900833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620692-T-G

72900965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620560-T-C

72901051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620476-T-C

72901051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620476-T-G

72901175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620363-A-G

72901175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3 prime UTR variant
orthologous variants: 20620363-A-T

72901410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20620123-A-G

72901426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20620107-T-C

72901492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20620036-C-G

http://identifiers.org/hco/9/GRCh38#72901735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20619869-C-A

72901968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20619668-C-T

72902242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20619400-T-C

72902416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20619232-T-G

72902614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20619025-C-T

http://identifiers.org/hco/9/GRCh38#72902730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20618928-C-A

72902891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20618763-G-A

72902892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20618762-T-G

http://identifiers.org/hco/9/GRCh38#72902959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20618697-C-A

72903014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20618649-G-A

72905552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617882-T-C

72905714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617720-A-G

72905830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617624-G-T

72905884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617567-A-G

72905903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617551-A-G

http://identifiers.org/hco/9/GRCh38#72905946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617512-C-A

72905946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617512-C-T

http://identifiers.org/hco/9/GRCh38#72906037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617421-A-C

72906037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20617421-A-G

http://identifiers.org/hco/9/GRCh38#72906042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617414-A-C

http://identifiers.org/hco/9/GRCh38#72906043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617413-A-C

72906054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617402-T-A

72906054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617402-T-C

72906115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617343-A-G

http://identifiers.org/hco/9/GRCh38#72906119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617339-C-A

72906119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617339-C-G

72906119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617339-C-T

http://identifiers.org/hco/9/GRCh38#72906120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617338-C-A

72906120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617338-C-T

72906121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617337-T-A

72906121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617337-T-C

72906121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617337-T-G

http://identifiers.org/hco/9/GRCh38#72906154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617301-C-A

72906154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617301-C-G

72906154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617301-C-T

http://identifiers.org/hco/9/GRCh38#72906164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617291-A-C

72906167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617288-A-T

http://identifiers.org/hco/9/GRCh38#72906177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20617279-C-A

72906177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20617279-C-T

72906685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20616809-T-A

72907717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20616744-T-C

72907772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20616693-C-G

72907800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20616662-G-A

72907878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20616585-G-A

http://identifiers.org/hco/9/GRCh38#72909522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20614259-C-A

72909522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614259-C-T

72909544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614240-T-C

72909590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614199-G-A

72909590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614199-G-T

72909591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614198-G-A

72909591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20614198-G-T

72909833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613972-T-C

http://identifiers.org/hco/9/GRCh38#72909841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20613964-A-C

72909841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613964-A-G

72909841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613964-A-T

http://identifiers.org/hco/9/GRCh38#72909846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20613957-A-C

72909846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613957-A-G

http://identifiers.org/hco/9/GRCh38#72909884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20613919-C-A

72909884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613919-C-T

72910013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613771-G-T

72910042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613741-T-C

http://identifiers.org/hco/9/GRCh38#72910120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20613673-C-A

72910174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613617-T-C

72910319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613509-T-C

72910334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613493-G-A

http://identifiers.org/hco/9/GRCh38#72910335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20613492-A-C

72910722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613142-A-G

72910802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20613062-G-A

72910961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612877-C-G

72910961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612877-C-T

72911502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612299-C-G

72911563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612250-A-G

72911709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612102-G-A

72911709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612102-G-T

http://identifiers.org/hco/9/GRCh38#72911710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20612101-C-A

72911778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20612031-C-T

http://identifiers.org/hco/9/GRCh38#72911823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20611989-C-A

72911823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611989-C-T

72911870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611957-A-G

72911942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611890-G-A

72911989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense variant
orthologous variants: 20611844-A-G

72912090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: synonymous variant
orthologous variants: 20611743-G-A

72912090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense variant
orthologous variants: 20611743-G-C

http://identifiers.org/hco/9/GRCh38#72912176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20611656-C-A

72912176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611656-C-T

72912223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611623-C-T

72912282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611522-A-G

72912420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611407-T-C

http://identifiers.org/hco/9/GRCh38#72912476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20611352-C-A

72912476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20611352-C-T

72915808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20609649-T-C

72915925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20609532-G-C

72916037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20609421-A-G

72916535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20608918-A-T

http://identifiers.org/hco/9/GRCh38#72916802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608319-C-A

72916802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20608319-C-T

http://identifiers.org/hco/9/GRCh38#72916833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608290-A-C

72916882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20608248-G-T

http://identifiers.org/hco/9/GRCh38#72916896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608236-C-A

72916896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20608236-C-T

http://identifiers.org/hco/9/GRCh38#72916978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608154-C-A

72916978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 20608154-C-T

http://identifiers.org/hco/9/GRCh38#72917047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608085-C-A

http://identifiers.org/hco/9/GRCh38#72917096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20608036-C-A

72917167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607911-T-C

http://identifiers.org/hco/9/GRCh38#72917168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20607910-C-A

72917168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607910-C-G

72917168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607910-C-T

72917179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607899-T-A

72917215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607875-C-T

72917231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607859-T-C

http://identifiers.org/hco/9/GRCh38#72917248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20607842-A-C

72917248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607842-A-G

72917854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607305-G-T

http://identifiers.org/hco/9/GRCh38#72917961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20607216-A-C

72918010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20607170-A-G

72918391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606815-T-C

72918597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606631-A-G

72918597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606631-A-T

72918648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606586-A-G

72918700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606537-A-G

72918850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606388-G-A

72918850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606388-G-T

http://identifiers.org/hco/9/GRCh38#72918911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20606327-C-A

72918911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606327-C-T

72918913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606325-A-G

72919108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606244-A-T

72919231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606124-A-G

72919239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606116-T-C

72919267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606095-C-T

72919272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20606090-C-T

72919601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605878-T-C

72919677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605837-C-T

72919741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605766-A-T

72919780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605732-A-G

72919780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605732-A-T

72919987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605540-G-A

http://identifiers.org/hco/9/GRCh38#72920066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20605461-C-A

72920153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605389-G-C

72920191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20605357-C-T

72920588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20604852-C-T

72920589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20604851-G-A

72920589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20604851-G-C

72920682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20604776-G-T

72922218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603779-A-G

http://identifiers.org/hco/9/GRCh38#72922264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20603728-A-C

72922269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603723-T-C

72922789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603374-C-G

72922877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603251-A-G

72922898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603234-G-A

72922898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20603234-G-C

72923467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602727-C-T

72923525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602672-G-T

http://identifiers.org/hco/9/GRCh38#72923623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20602572-C-A

72923710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602486-T-C

http://identifiers.org/hco/9/GRCh38#72923713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20602483-C-A

72923713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602483-C-T

72923724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602464-A-G

72923761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602429-A-G

72923761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602429-A-T

72923841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20602352-G-T

72923861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602332-T-G

72923886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602306-G-C

72923886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602306-G-T

72923898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602294-A-G

72923902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602290-A-G

72923939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602253-T-C

http://identifiers.org/hco/9/GRCh38#72923940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20602252-C-A

72923940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602252-C-T

72923965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602222-T-C

72923965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20602222-T-G

http://identifiers.org/hco/9/GRCh38#72924029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20602177-C-A

72924107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20602099-T-C

http://identifiers.org/hco/9/GRCh38#72924125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20602081-A-C

72924192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20602028-T-A

72924192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20602028-T-C

72924192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20602028-T-G

72924202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20602018-A-G

72924203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20602017-G-T

72924253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601968-A-G

72924322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601908-G-A

72924322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601908-G-C

72924401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601832-A-G

72924671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601619-G-A

72924702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601582-G-A

72924797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601486-T-A

72924945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601356-T-C

72925148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601175-T-G

72925255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20601081-G-T

http://identifiers.org/hco/9/GRCh38#72925368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20600969-C-A

72925368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600969-C-T

72925373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600964-G-A

72925373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600964-G-C

72925373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600964-G-T

72925402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20600935-T-C

72925402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20600935-T-G

72925408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600920-A-G

72925410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600918-C-T

72925420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600908-G-C

72925430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600867-T-C

72925536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20600763-G-A

72925647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600651-T-C

72925654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600643-A-T

72925738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600571-G-A

72925738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600571-G-T

72926120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20600105-A-G

72926289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599924-T-C

72926488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599719-G-A

72926582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599628-A-T

72926897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599317-A-G

72926897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599317-A-T

72926910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599304-A-T

72926954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599260-G-A

72926954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599260-G-T

72926958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599256-G-T

http://identifiers.org/hco/9/GRCh38#72926968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20599246-C-A

http://identifiers.org/hco/9/GRCh38#72927015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20599192-C-A

72927015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599192-C-T

72927029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599179-T-A

72927029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599179-T-C

72927029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599179-T-G

http://identifiers.org/hco/9/GRCh38#72927043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20599165-A-C

72927043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599165-A-G

72927043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599165-A-T

72927048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599160-G-A

72927048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599160-G-C

72927048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599160-G-T

http://identifiers.org/hco/9/GRCh38#72927055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20599153-C-A

72927055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20599153-C-T

http://identifiers.org/hco/9/GRCh38#72927193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20599015-C-A

72927193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20599015-C-T

72927262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598968-G-A

72927262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598968-G-T

72927265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598965-G-T

72927266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598964-A-T

72927366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598931-A-G

72927666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598683-C-T

72927864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598399-C-G

http://identifiers.org/hco/9/GRCh38#72927873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20598390-A-C

72927881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598382-A-T

http://identifiers.org/hco/9/GRCh38#72927959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20598323-A-C

72928122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598160-A-G

72928239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598038-A-T

72928263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20598020-T-A

72928506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20597820-T-G

72928591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20597741-G-A

72928615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20597721-A-G

72928671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20597665-A-T

72928821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20597527-G-T

72929126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596785-A-G

72929127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596784-A-G

72929427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596512-G-A

72929532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596420-A-G

72929714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596266-G-C

72929764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596238-G-T

72929866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596135-C-T

http://identifiers.org/hco/9/GRCh38#72929867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20596134-A-C

72929962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20596040-G-A

72930154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595901-A-T

72930281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595782-A-G

72930444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595647-A-T

72930483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595609-C-G

72930553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595587-G-A

72930662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595533-T-C

http://identifiers.org/hco/9/GRCh38#72930810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20595457-A-C

72930810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595457-A-G

72930810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595457-A-T

72930840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595427-G-A

72930846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595421-T-C

http://identifiers.org/hco/9/GRCh38#72930860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20595401-C-A

72930860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595401-C-T

72930880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 20595381-G-A

72931067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20595194-A-T

72931076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595185-A-G

72931086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20595176-A-G

http://identifiers.org/hco/9/GRCh38#72931139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20595130-C-A

72931139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595130-C-T

72931170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595096-T-A

72931170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595096-T-C

72931170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595096-T-G

72931183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20595085-A-G

72935200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592559-T-G

72935219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592540-A-T

72935346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592427-T-C

72935395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592392-G-T

72935534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592258-A-T

72935593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592197-G-A

72935624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592185-G-T

72935668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592148-A-G

72935703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592108-C-T

72935736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592076-A-G

72935744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592068-G-A

72935744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592068-G-C

72935744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592068-G-T

72935785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592029-T-G

http://identifiers.org/hco/9/GRCh38#72935787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20592027-A-C

http://identifiers.org/hco/9/GRCh38#72935805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20592009-A-C

72935805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20592009-A-G

72935861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591951-A-G

72935902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591908-G-A

72935902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591908-G-C

72936124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591701-G-A

72936191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591638-C-G

72936192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591637-A-G

72936206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591623-C-T

72936239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591591-T-C

72936283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591549-A-T

http://identifiers.org/hco/9/GRCh38#72936311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20591523-C-A

72936311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591523-C-T

72936313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20591521-T-C

http://identifiers.org/hco/9/GRCh38#72937029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20590650-A-C

72937108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590570-T-C

72937188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590492-T-C

http://identifiers.org/hco/9/GRCh38#72937551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20590361-C-A

72937684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590219-C-G

72937825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590090-T-C

72937825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590090-T-G

72937831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590084-G-A

72937910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20590008-C-T

72937992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20589928-T-A

72938094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20589822-C-G

72940068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588441-T-C

72940068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588441-T-G

72940179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20588348-T-G

72940200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20588327-A-G

72940215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20588312-C-T

http://identifiers.org/hco/9/GRCh38#72940225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20588302-A-C

72940225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20588302-A-G

72940263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588264-G-A

72940263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588264-G-C

72940263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588264-G-T

72940297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588232-A-T

72940317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588210-A-T

72940382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588145-T-C

72940386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588143-G-T

72942679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20588033-C-T

72942728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20587980-T-C

72942874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20587844-T-C

72944690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585812-G-T

72944725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585779-T-C

72944740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585764-A-G

72944770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585744-T-C

72944779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585735-T-A

72944991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585519-C-T

72945109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585406-T-G

72945208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585257-G-A

72945246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585218-A-G

72945389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585101-G-T

72945441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585054-T-C

72945461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585034-G-C

72945613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584885-T-C

72945739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584759-G-A

72945949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584558-C-T

72945950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584557-T-A

72945950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584557-T-G

72947625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584093-T-C

72947712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584008-T-C

72947765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583954-A-G

72947998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583718-A-G

72948114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583597-G-A

72948137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583574-A-G

72948299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583411-A-G

72948313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583399-C-T

72949217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582936-A-G

72949361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582791-A-G

72949392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582766-A-G

72949548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582643-C-T

72949835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582431-T-A

http://identifiers.org/hco/9/GRCh38#72950283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20582052-A-C

72950562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20581845-C-T

72950633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20581778-C-T

72950637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20581774-G-A

72950732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20581687-C-T

72951268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20581213-A-T

72951503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580959-T-A

http://identifiers.org/hco/9/GRCh38#72951560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20580902-A-C

72951847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580600-C-T

72952018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580437-A-G

72952022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580433-A-T

http://identifiers.org/hco/9/GRCh38#72952096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20580363-A-C

72952106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580353-A-G

72952176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580262-T-C

72952483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20579926-A-G

72953204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20579183-A-G

72953462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578919-T-A

72953650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578747-C-G

72953737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578668-C-T

72953829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578569-A-G

72953981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578412-C-T

72954001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578392-G-T

72954044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578352-A-G

72954351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20578088-A-G

72954531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20577901-T-C

72954677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20577759-A-G

72955116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20577341-C-T

72956400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575653-A-G

72956400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575653-A-T

72956566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575458-A-G

72956598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575416-C-T

72956903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575146-A-G

72956937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20575107-G-A

72957165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20574884-T-C

72957188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20574863-C-T

72960243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561500-G-A

72960256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561487-C-T

72960382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561357-C-T

72960412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561348-C-T

72960461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561296-T-A

http://identifiers.org/hco/9/GRCh38#72960469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20561288-C-A

72960679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561101-A-T

72960742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20561038-T-G

72960861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20560942-A-G

72960914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20560894-T-A

72960976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20560831-A-T

72961090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20560720-T-A

72961101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20560709-C-T

72969609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20556503-G-A

72969774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20556337-T-C

http://identifiers.org/hco/9/GRCh38#72969968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20556153-A-C

72969968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20556153-A-G

72970215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20555931-T-C

72970723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20555347-T-C

72970824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20555257-C-T

http://identifiers.org/hco/9/GRCh38#72970826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20555255-C-A

72970860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20555223-A-G

72971242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554849-T-A

72971242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554849-T-C

72971242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554849-T-G

72971335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554761-T-C

72971346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554750-C-T

http://identifiers.org/hco/9/GRCh38#72971356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20554740-C-A

72971356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554740-C-T

72971387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554708-T-A

72971564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554526-T-C

http://identifiers.org/hco/9/GRCh38#72971581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20554509-A-C

72971581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554509-A-G

72971750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554345-G-A

72971900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554203-G-A

72971920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554186-T-C

72971942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554165-C-G

72971982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554120-T-C

72971987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554115-T-C

72972009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554093-T-G

72972020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554082-A-G

72972034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20554068-A-G

72972129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553997-T-C

72972173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553950-T-A

72972173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553950-T-C

72972173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553950-T-G

72972207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553924-T-C

72972219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553911-T-A

72972219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553911-T-G

72972282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553854-C-G

72972283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553853-A-T

72972297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553839-A-G

72972338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20553798-G-A

72972534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20551296-T-A

72972545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20551285-G-C

72972580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20551258-T-C

http://identifiers.org/hco/9/GRCh38#72972656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20551185-C-A

72972656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20551185-C-G

72972656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20551185-C-T

http://identifiers.org/hco/9/GRCh38#72972698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20544669-C-A

72972909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20544444-G-A

72972909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20544444-G-T

http://identifiers.org/hco/9/GRCh38#72972999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20544351-A-C

http://identifiers.org/hco/9/GRCh38#72973262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20544116-C-A

72974048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543317-C-T

72974269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543116-A-G

72974295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543113-C-G

72974345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543090-A-G

72974363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543072-A-G

72974385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20543051-A-T

72974437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20542987-T-C

72974686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20542719-T-C

72975568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20541459-C-T

http://identifiers.org/hco/9/GRCh38#72975569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20541458-A-C

72975763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20541260-T-G

72975894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20541131-A-G

72976049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20540974-A-G

72977593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539487-T-C

72977593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539487-T-G

72977621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539457-A-T

72977647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539431-T-A

72977698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539394-A-G

72977839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539254-A-G

72977839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539254-A-T

72978035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20539111-C-T

72978271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20538263-C-T

http://identifiers.org/hco/9/GRCh38#72978330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20538204-C-A

72978376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20538151-A-G

72978461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20538062-T-C

72978461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20538062-T-G

72978619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537904-A-T

72978626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537886-G-A

72978903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537605-G-A

http://identifiers.org/hco/9/GRCh38#72979046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20537463-C-A

72979046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537463-C-G

http://identifiers.org/hco/9/GRCh38#72979071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20537438-A-C

72979095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537408-C-T

72979129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20537372-G-T

http://identifiers.org/hco/9/GRCh38#72979171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20537299-C-A

72979407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20536714-G-A

72979550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20536567-G-T

72979607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20536511-T-C

72979628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20536490-T-C

72979779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20536289-T-A

http://identifiers.org/hco/9/GRCh38#72980039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20535961-C-A

72980121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20535849-G-C

72980131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20535839-C-T

72980152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20535814-A-G

72980467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20535126-A-G

72980517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20535086-T-C

72980965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534639-A-G

72981060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534548-C-T

http://identifiers.org/hco/9/GRCh38#72981098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20534511-C-A

72981098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534511-C-T

72981200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534442-T-C

72981330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534327-C-G

72981331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534326-T-A

72981331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534326-T-G

72981338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534322-C-T

72981348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534310-G-A

72981348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534310-G-T

72981421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20534240-T-G

72981712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533950-A-G

72981907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533773-T-G

72982105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533559-A-G

72982119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533550-T-C

72982625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533065-T-C

72982626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20533064-G-A

72982826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20532871-T-C

72982832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20532865-A-G

72982914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20532780-G-A

72983445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20530599-G-A

72983663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20530047-C-T

72983819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20529892-T-C

72984023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20529689-G-A

72984238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20529504-A-T

72984524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20529259-A-G

72984987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20527232-T-C

72985029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20527192-G-C

72985043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20527177-A-G

72985064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20527158-T-C

72985074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20527148-T-G

72985335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526894-C-T

72985356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526873-A-G

72985398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526832-A-G

72985434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526798-A-G

http://identifiers.org/hco/9/GRCh38#72985504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20526736-C-A

72985584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526655-T-C

72985600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526639-A-G

72985769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526465-T-C

72985988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20526249-C-T

72986275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20525958-T-C

72986275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20525958-T-G

72986289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20525945-A-T

http://identifiers.org/hco/9/GRCh38#72986351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20525879-C-A

http://identifiers.org/hco/9/GRCh38#72986470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20525769-C-A

72986470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20525769-C-T

72986537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20525717-C-T

72987329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20524852-T-G

72988219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20524262-G-A

72988335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20524168-T-G

http://identifiers.org/hco/9/GRCh38#72988476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20524049-C-A

72988529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523995-T-C

http://identifiers.org/hco/9/GRCh38#72988632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20523916-A-C

72988796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523797-C-T

72988825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523774-A-G

72988888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523711-T-G

72989066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523530-T-G

72989082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523517-C-G

72989242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20523390-A-G

72991202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20522628-C-T

http://identifiers.org/hco/9/GRCh38#72991494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20522310-C-A

http://identifiers.org/hco/9/GRCh38#72992022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20521826-C-A

72992060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20521802-T-C

http://identifiers.org/hco/9/GRCh38#72992108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20521755-A-C

72992154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20521706-T-C

72992823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20521041-T-C

72992998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520883-T-C

http://identifiers.org/hco/9/GRCh38#72993096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20520783-A-C

72993096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520783-A-G

http://identifiers.org/hco/9/GRCh38#72993221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20520657-A-C

72993339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520552-T-C

72993555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520357-A-T

72993634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520280-G-T

72993636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520278-C-T

72993734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520195-A-G

72993736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20520193-C-T

72994133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519861-G-A

72994264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519761-G-A

72994293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519735-C-T

72995979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519366-T-G

72996007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519337-C-T

72996281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519076-T-C

72996283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519074-G-A

72996343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519013-G-A

72996343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20519013-G-T

72996502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518872-G-A

http://identifiers.org/hco/9/GRCh38#72996528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20518844-C-A

72996868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518675-A-G

72997024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518514-G-C

72997024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518514-G-T

72997129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518406-A-G

72997196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518329-T-C

72997298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518243-G-A

72997329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518213-G-A

72997376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20518173-G-T

72997613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517945-G-T

72997666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517729-A-G

72997693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517702-G-A

72997822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517602-G-A

72997829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517595-G-A

72997840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517584-A-T

72998345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20517094-A-G

73009634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20516247-T-C

73009657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20516224-C-T

http://identifiers.org/hco/9/GRCh38#73009711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20516170-A-C

73009711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20516170-A-G

73009743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20516142-A-G

73009855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20516051-A-G

73009954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20515954-A-G

73009985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20515939-A-T

73010020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20515900-G-A

73010070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20515857-G-A

73010070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20515857-G-T

73010713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20515253-T-C

73010777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20515212-T-C

73010979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514989-A-T

73011040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514928-T-C

73011194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514562-G-A

73011299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514459-A-G

73011302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514445-A-G

73011508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514247-T-A

73011589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20514166-T-C

73011827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513928-C-T

73012009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513737-C-T

73012063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513692-A-T

73012168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513594-A-G

73012206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513553-A-G

73012285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513470-C-T

73012302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513449-T-C

73012306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513445-A-G

73012658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513103-G-C

73012751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20513015-T-G

73012780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512988-G-A

73012878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512891-G-A

73012985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512801-A-G

73013236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512597-G-A

73013270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512578-G-A

73013349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512510-G-C

73013416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512431-C-T

73013581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512253-G-A

73013786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20512053-A-T

73014644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20510653-T-C

73014662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20510627-C-T

73014715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20510570-G-A

73014715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20510570-G-T

73014956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20510334-T-C

73015427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20509894-A-G

73015507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20509814-C-T

73015547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20509774-A-G

73015561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20509760-G-A

73031991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20475867-C-G

73031995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20475863-T-C

73032208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20475659-T-C

73032449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20475159-T-A

73032449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20475159-T-C

73034858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20474290-G-A

73034906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20474252-T-C

73035213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20474007-G-A

73035273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473949-A-G

73035301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473921-T-C

73035353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473871-G-A

73035402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473826-G-A

73035406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473822-T-C

73035506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473748-T-A

73035649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473643-T-C

73035664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473628-A-G

73035675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473617-A-G

73035675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473617-A-T

http://identifiers.org/hco/9/GRCh38#73035693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20473599-C-A

73035802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473486-G-A

73035872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20473182-G-A

http://identifiers.org/hco/9/GRCh38#73035887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20473167-C-A

73036084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472997-A-G

73036131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472967-T-C

http://identifiers.org/hco/9/GRCh38#73036164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20472935-C-A

73036195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472905-A-G

73036265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472847-A-T

73036512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472610-G-A

73036595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472503-A-G

73036622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472472-G-A

73036639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472455-T-C

73036716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472391-A-G

73036851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20472261-T-A

73037485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20471267-A-G

73037513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20471239-C-G

73037875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470905-G-A

73037875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470905-G-C

73038006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470795-C-T

73038016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470785-A-G

73038067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20470722-A-T

73038072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20470717-A-G

73038072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20470717-A-T

73038223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470567-T-C

73038430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, undefined
orthologous variants: 20470389-A-G

73038477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470353-G-A

73038493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470337-T-C

73038501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470331-T-C

http://identifiers.org/hco/9/GRCh38#73038574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20470262-C-A

http://identifiers.org/hco/9/GRCh38#73038681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20470166-C-A

73038681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 20470166-C-G

73038751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470105-C-G

73038751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470105-C-T

73038782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470075-T-C

73038848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470016-T-A

73038848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470016-T-C

73038848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470016-T-G

73038850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20470014-T-C

73038901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469969-C-T

73039038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469844-G-T

http://identifiers.org/hco/9/GRCh38#73039202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20469688-C-A

http://identifiers.org/hco/9/GRCh38#73039355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20469574-A-C

73039501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469428-G-A

73039501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469428-G-C

73039615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469370-C-G

73039629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron variant
orthologous variants: 20469350-C-T

73057849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20462423-C-T

73057941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20462333-A-G

73058058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20462235-C-T

73058059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20462234-G-A

73058085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20462208-A-G

73058852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20461801-T-C

73059090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20455012-T-A

73059094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20455008-A-G

73059106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454996-T-G

73059160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454942-C-T

73059202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454897-A-T

73059503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454646-G-A

73059864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454271-G-A

73059889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454244-A-G

73059972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454173-T-A

73059995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454152-C-T

73060077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454078-C-T

73060111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20454047-G-C

73060384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20450589-A-T

73061363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20450006-C-T

73061488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449882-A-G

73061595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449772-A-G

73061712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449692-C-T

73061885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449556-C-T

73061936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449512-A-G

73061947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449503-G-A

73062603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20449155-C-T

73064452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20447345-C-T

73064679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20447151-T-G

73064683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20447147-A-G

http://identifiers.org/hco/9/GRCh38#73065922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20446666-A-C

73066062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20446430-G-C

73073102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20446042-C-T

73073272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445877-T-C

73073552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445660-G-T

73073556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445656-C-T

73073694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445518-A-G

73073718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445495-C-T

73073854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20445375-C-G

http://identifiers.org/hco/9/GRCh38#73073980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#20445264-C-A

73074229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20445024-G-A

73074280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20444973-G-A

73074298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20444955-T-C

73074334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20444919-T-C

73074413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20444840-T-C

73074498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20444756-C-T

73074582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20444652-T-C

73074787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443827-T-C

73074801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443813-A-T

73074806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443808-C-T

73074820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443794-T-C

73074849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443765-C-T

http://identifiers.org/hco/9/GRCh38#73074868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20443746-A-C

73074998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443625-G-T

73075066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20443556-G-A

73076319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20440343-T-C

73076343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20440319-T-C

73076344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20440318-G-T

73076505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20432387-T-A

73076571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20432330-A-G

http://identifiers.org/hco/9/GRCh38#73076784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20432197-A-C

73076931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20432132-A-T

73076963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20432107-G-A

73077464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431679-G-T

73077582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431579-C-G

73077612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431509-T-C

73077693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431433-A-G

73077693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431433-A-T

73077811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20431320-G-A

73079713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20428359-T-C

73079737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20428331-A-G

http://identifiers.org/hco/9/GRCh38#73080198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#20428059-A-C

73080218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20428039-A-G

73080219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20428038-G-T

73080243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20428014-G-A