http://identifiers.org/hco/7/GRCh38#128790789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29396023-C-A

128790789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5 prime UTR variant
orthologous variants: 29396023-C-T

128790861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5 prime UTR variant
orthologous variants: 29396079-G-A

128790870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5 prime UTR variant
orthologous variants: 29396088-G-A

128790870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5 prime UTR variant
orthologous variants: 29396088-G-T

128790993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396198-G-A

128790993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396198-G-C

128790993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396198-G-T

128791000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396205-G-A

128791000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396205-G-T

http://identifiers.org/hco/7/GRCh38#128791027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29396228-C-A

128791027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29396228-C-G

128791028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29396229-T-A

128791028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29396229-T-C

128791028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29396229-T-G

128791061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396262-T-C

128791061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396262-T-G

128791067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396268-G-A

128791067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396268-G-T

128791074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396286-T-C

128791074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396286-T-G

http://identifiers.org/hco/7/GRCh38#128791124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29396321-A-C

128791124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396321-A-G

128791124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396321-A-T

128791136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396333-G-A

128791277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396471-C-G

128791277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396471-C-T

128791306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396501-G-A

128791306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29396501-G-T

http://identifiers.org/hco/7/GRCh38#128791443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29396635-C-A

128791443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29396635-C-G

128791443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29396635-C-T

128791678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29396838-T-C

128791726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29396884-A-G

http://identifiers.org/hco/7/GRCh38#128791796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29396939-C-A

128791796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29396939-C-T

128791915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397073-A-G

128791915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397073-A-T

http://identifiers.org/hco/7/GRCh38#128791931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29397098-C-A

128791931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397098-C-T

128792085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397234-T-C

128792085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397234-T-G

128792243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397409-T-A

128792243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397409-T-C

128792280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397438-G-A

128792280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397438-G-C

128792280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397438-G-T

128792311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397469-T-A

128792311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397469-T-C

128792311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29397469-T-G

128792396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29397554-C-G

128792445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397603-G-C

128792445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397603-G-T

http://identifiers.org/hco/7/GRCh38#128792458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29397616-C-A

128792458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397616-C-T

http://identifiers.org/hco/7/GRCh38#128792488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29397639-C-A

128792629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397777-C-G

128792629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29397777-C-T

128792819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29397964-G-A

128793266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29398339-G-A

128793403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29398647-C-T

128794143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399019-T-A

128794148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399024-G-T

http://identifiers.org/hco/7/GRCh38#128794212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29399082-C-A

128794212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399082-C-G

128794212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399082-C-T

128794247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399116-G-A

128794339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399191-G-A

128794339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399191-G-C

http://identifiers.org/hco/7/GRCh38#128794454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29399300-C-A

128794454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: synonymous variant
orthologous variants: 29399300-C-G

128794454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: synonymous variant
orthologous variants: 29399300-C-T

128794636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399482-C-T

128794656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399502-T-C

128794684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399524-C-T

128794989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399788-C-T

128795177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399966-G-A

128795181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29399970-G-A

128795402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400156-C-T

128795537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400293-T-G

128795541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400297-T-A

128795541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400297-T-C

128795541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400297-T-G

128795975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29400835-G-A

128796329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401353-A-G

128796414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29401428-C-T

128796434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, undefined
orthologous variants: 29401448-G-A

128796759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401790-T-A

128796767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401798-A-G

128796767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401798-A-T

128796834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401855-C-G

128796834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401855-C-T

128796850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401870-T-G

128796891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401910-G-A

128796891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29401910-G-T

128797376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29402255-G-A

128797578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29402421-T-A

http://identifiers.org/hco/7/GRCh38#128797694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29402537-C-A

128797809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29402640-A-G

128797858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29402699-C-T

128798003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29402818-C-T

128800773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405610-T-C

128800820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405661-G-C

http://identifiers.org/hco/7/GRCh38#128801095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29405762-A-C

128801114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405781-A-G

128801127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405794-A-T

http://identifiers.org/hco/7/GRCh38#128801146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29405813-C-A

128801146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405813-C-T

128801160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405822-A-G

128801160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron variant
orthologous variants: 29405822-A-T

128801292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29405976-G-C

128801479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29406160-T-C

128801597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406278-T-C

128801597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406278-T-G

http://identifiers.org/hco/7/GRCh38#128801651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29406306-C-A

128801651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406306-C-T

128801805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406326-G-A

128802202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406709-G-T

128802221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406723-T-G

128802940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407447-G-A

128804532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409096-A-G

128804532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409096-A-T

128804567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409131-G-A

128804567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409131-G-T

128804610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409172-T-C

128804672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29409246-A-G

128804750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29409324-G-A

128804750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29409324-G-C

128804750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29409324-G-T

http://identifiers.org/hco/7/GRCh38#128804800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29409348-C-A

128804800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409348-C-T

128804801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409349-A-G

http://identifiers.org/hco/7/GRCh38#128804802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29409350-C-A

128804928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409474-A-G

128805207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409931-G-C

http://identifiers.org/hco/7/GRCh38#128805217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29409941-C-A

128805217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409941-C-T

128805287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410009-G-T

128805314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410029-A-G

128805314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410029-A-T

128805320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410035-A-G

128805563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410278-G-A

128805563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410278-G-T

128805568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410283-T-C

128805657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410378-T-C

128806021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411488-G-A

128806021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411488-G-T

http://identifiers.org/hco/7/GRCh38#128806218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29411690-C-A

128806218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411690-C-T

128806296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29411768-T-C

128806374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29411846-T-G

128806436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411907-G-T

http://identifiers.org/hco/7/GRCh38#128806443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29411914-C-A

http://identifiers.org/hco/7/GRCh38#128806493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29412006-C-A

128806493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29412006-C-T

128806525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29412201-G-T

128806605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29412291-G-A

128806605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29412291-G-C

http://identifiers.org/hco/7/GRCh38#128806661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29412337-C-A

128806661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29412337-C-T

128806947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412610-G-A

128806947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412610-G-C

128806954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412620-G-A

128806954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412620-G-C

128806954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412620-G-T

http://identifiers.org/hco/7/GRCh38#128807524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29413065-C-A

128807524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29413065-C-G

128807524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29413065-C-T

http://identifiers.org/hco/7/GRCh38#128807625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29413154-C-A

http://identifiers.org/hco/7/GRCh38#128807703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29413212-C-A

128807703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29413212-C-T

http://identifiers.org/hco/7/GRCh38#128807705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29413214-C-A

128807898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413389-G-A

128807898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413389-G-C

128807925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413418-G-T

128808233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413617-C-T

128808248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413631-G-C

128808248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413631-G-T

http://identifiers.org/hco/7/GRCh38#128808537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29413865-A-C

128808795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414127-C-T

128808977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414369-G-A

128809035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414428-G-A

http://identifiers.org/hco/7/GRCh38#128809060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414454-C-A

http://identifiers.org/hco/7/GRCh38#128809099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414485-C-A

128809099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414485-C-G

128809099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414485-C-T

http://identifiers.org/hco/7/GRCh38#128809225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414590-C-A

128809225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414590-C-T

128809272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414618-G-A

128809272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414618-G-T

128809309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414642-G-A

128809309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414642-G-C

128809309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414642-G-T

128809320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414653-T-A

128809320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414653-T-C

128809320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414653-T-G

128809326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414659-G-A

128809326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414659-G-T

http://identifiers.org/hco/7/GRCh38#128809355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414701-A-C

128809355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414701-A-G

128809355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414701-A-T

128809376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414720-A-G

http://identifiers.org/hco/7/GRCh38#128809377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414721-A-C

128809392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414736-A-T

http://identifiers.org/hco/7/GRCh38#128809411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414751-C-A

128809411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414751-C-T

http://identifiers.org/hco/7/GRCh38#128809412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414752-A-C

128809412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29414752-A-G

128809611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29414946-A-G

http://identifiers.org/hco/7/GRCh38#128809651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29414987-C-A

128809651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29414987-C-G

128809651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29414987-C-T

128809660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414996-G-A

128809660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414996-G-T

128809724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415066-G-T

128809932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415252-C-T

128810043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415346-G-C

128810043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415346-G-T

128810062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415369-A-T

http://identifiers.org/hco/7/GRCh38#128810101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29415402-C-A

128810101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415402-C-T

http://identifiers.org/hco/7/GRCh38#128810234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29415525-A-C

http://identifiers.org/hco/7/GRCh38#128810262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29415553-A-C

128810262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29415553-A-T

128810577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415841-A-G

128810786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416075-T-C

128810880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416165-G-C

http://identifiers.org/hco/7/GRCh38#128811278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#29416545-C-A

128811278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29416545-C-T

http://identifiers.org/hco/7/GRCh38#128811462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29416725-C-A

http://identifiers.org/hco/7/GRCh38#128811814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29417082-C-A

128811814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29417082-C-G

128811814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29417082-C-T

128811818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417086-G-A

128811850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29417118-C-T

128811956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29417224-C-T

128812002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417270-A-G

128812003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29417271-C-T

128812083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417351-G-A

128812152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417420-C-T

128812227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417492-G-A

128812334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417599-G-A

128812334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417599-G-C

128812410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417671-G-A

http://identifiers.org/hco/7/GRCh38#128812575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29417813-A-C

128812575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417813-A-G

128812575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417813-A-T

http://identifiers.org/hco/7/GRCh38#128812602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29417831-C-A

128812602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417831-C-G

128812602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29417831-C-T

http://identifiers.org/hco/7/GRCh38#128812740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29417963-C-A

128812740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29417963-C-G

128812903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29418126-A-G

128812904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29418127-T-C

128813017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418189-A-G

http://identifiers.org/hco/7/GRCh38#128813018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29418190-C-A

128813057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418219-T-A

128813057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418219-T-G

http://identifiers.org/hco/7/GRCh38#128813063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29418225-A-C

128813063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418225-A-G

128813073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418234-A-G

128813408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418489-G-A

128813468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418560-G-A

128813475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418567-A-G

128813551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418633-G-A

128813611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418692-C-G

128813611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418692-C-T

http://identifiers.org/hco/7/GRCh38#128814542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29419022-C-A

128814542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419022-C-T

http://identifiers.org/hco/7/GRCh38#128814549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29419029-C-A

128814549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419029-C-T

128814629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419092-T-C

128814742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29419205-G-A

128814769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29419232-C-T

http://identifiers.org/hco/7/GRCh38#128814912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29419375-C-A

128814912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29419375-C-T

128814928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419391-T-C

128814953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419418-A-T

128815066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419501-A-T

128815175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419549-A-T

128815184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419558-G-A

128815249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419638-A-G

128815263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419652-G-A

128815490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419862-G-A

128815490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419862-G-T

128815503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419875-G-T

http://identifiers.org/hco/7/GRCh38#128815516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29419888-C-A

128815519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419891-G-A

128815580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419953-G-A

128815580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419953-G-C

128815714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29420081-A-G

128815725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29420092-G-A

128815725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 29420092-G-T

128815892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29420225-C-G

128815892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29420225-C-T

http://identifiers.org/hco/7/GRCh38#128815943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29420276-C-A

http://identifiers.org/hco/7/GRCh38#128816055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29420376-A-C

128816132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420450-C-T

128816249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420564-C-T

128816431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420691-C-T

128816547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420800-T-A

128816583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420835-G-A

128816660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420907-C-T

http://identifiers.org/hco/7/GRCh38#128817102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29421285-A-C

128817102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421285-A-G

128817251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421433-C-T

http://identifiers.org/hco/7/GRCh38#128817284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29421466-C-A

128817628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421857-T-G

http://identifiers.org/hco/7/GRCh38#128817707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29421945-C-A

128817707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421945-C-T

128817775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422007-T-A

128817775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29422007-T-C

http://identifiers.org/hco/7/GRCh38#128818018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29422191-C-A

128818018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422191-C-T

128818079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422263-G-A

128818079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422263-G-T

128818083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422267-T-C

128818122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422308-G-A

128818122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29422308-G-T

http://identifiers.org/hco/7/GRCh38#128818303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29422414-C-A

128818303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422414-C-T

128818422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422526-A-T

http://identifiers.org/hco/7/GRCh38#128818912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29422987-A-C

http://identifiers.org/hco/7/GRCh38#128819123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29423349-C-A

128819489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29423695-C-G

128819638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29423944-C-T

128819668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29423974-T-A

128819744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29424044-A-G

128819829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29424562-A-G

128821207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426053-T-C

128821212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426058-G-C

http://identifiers.org/hco/7/GRCh38#128821664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29426486-C-A

http://identifiers.org/hco/7/GRCh38#128821673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29426495-C-A

128821677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426499-A-T

128821716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426538-T-C

128821723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426545-C-G

128821948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29426771-G-C

128822008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29426827-G-A

128822008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29426827-G-T

128822131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3 prime UTR variant
orthologous variants: 29426950-T-A

128822131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22225
most severe consequence: 3 prime UTR variant
orthologous variants: 29426950-T-C