188974706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351121-C-T

188974737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351157-A-G

188975058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351461-C-T

http://identifiers.org/hco/2/GRCh38#188975102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45351507-A-C

188975451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351834-C-T

188975452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351835-A-G

188975519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45351892-T-G

188975700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45352060-T-C

188975702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45352062-G-A

http://identifiers.org/hco/2/GRCh38#188976178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45352589-C-A

188976251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45352792-C-T

188976258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45352799-G-T

188976292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45352839-G-A

188976578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45353023-T-C

188976769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45353204-A-G

188976879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45353312-A-T

188976900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45353333-A-G

188976913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45353346-T-C

188976988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45353507-G-A

188977460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354183-C-T

http://identifiers.org/hco/2/GRCh38#188977535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45354264-C-A

188977613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354342-A-G

188977639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354364-C-T

188977955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354674-G-A

188977969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354694-A-G

188977972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354697-A-G

188977985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354710-T-C

188977994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354719-G-A

188977994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354719-G-T

188978043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354752-G-A

188978043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354752-G-T

188978231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45354851-A-T

188978250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45354866-A-G

http://identifiers.org/hco/2/GRCh38#188978455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#45355051-C-A

188978482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45355078-T-C

188978687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45355264-C-T

188979055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45355623-T-C

http://identifiers.org/hco/2/GRCh38#188979435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45355975-C-A

http://identifiers.org/hco/2/GRCh38#188979442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45355980-C-A

188979908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45356401-G-A

188979994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45356482-A-G

188980399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45356881-T-G

188980438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45356918-A-G

188980438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45356918-A-T

188981531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45357290-A-G

188981649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45357404-C-T

188981794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45357525-C-T

188981878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45357614-T-A

188981950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45357691-A-G

188982187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45358290-T-C

188982204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45358307-C-T

188982342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45358432-G-A

188982826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45358963-T-G

http://identifiers.org/hco/2/GRCh38#188983029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45359080-C-A

188983088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359137-T-C

188983114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359162-T-C

188983242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359343-T-A

188983330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359429-G-A

188983342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359440-T-C

188983680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359613-A-T

188983753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359686-T-C

188984015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45359939-A-G

http://identifiers.org/hco/2/GRCh38#188984608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45360488-C-A

188984608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45360488-C-T

188984629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45360512-T-C

188984768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45360662-G-A

188984896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45360790-A-G

188985020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45360928-T-C

188985025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45360933-T-A

188985025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45360933-T-C

188985025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45360933-T-G

188985053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45360960-G-T

188985146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45361041-T-C

188985288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361189-G-A

http://identifiers.org/hco/2/GRCh38#188985354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45361261-C-A

188985354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361261-C-T

188985389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361294-A-G

188985402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361311-A-G

http://identifiers.org/hco/2/GRCh38#188985496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45361401-C-A

188985497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361402-A-G

188985581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361480-A-G

188985600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361497-A-G

188985613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361510-T-A

188985616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361513-G-T

188985750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45361651-T-C

188985778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 45361679-G-A

188985778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 45361679-G-C

188985949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361822-T-A

188985969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361842-T-G

188985973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361846-T-G

http://identifiers.org/hco/2/GRCh38#188986037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45361906-A-C

188986110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45361977-C-T

188986179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45362052-T-C

188986372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45362242-C-T

188986535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45362352-C-G

188986636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362446-T-C

188986677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45362498-G-A

188986677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45362498-G-T

188986945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362763-G-A

188986945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362763-G-T

188987011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362830-A-G

188987020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362839-C-G

188987023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362842-T-C

http://identifiers.org/hco/2/GRCh38#188987038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#45362857-C-A

188987038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362857-C-T

188987043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45362867-T-C

http://identifiers.org/hco/2/GRCh38#188987053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#45362877-C-A

188987053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 45362877-C-T

188987232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45363028-T-C

188987291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45363088-T-C

188987669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364124-G-A

188987669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364124-G-T

http://identifiers.org/hco/2/GRCh38#188987735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45364178-C-A

188987735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364178-C-T

188987791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364232-A-G

188987897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364328-A-G

188987961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364394-A-G

188987970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364403-T-G

188988148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364587-T-C

188988360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364748-G-A

188988399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364787-G-A

188988399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364787-G-C

188988399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364787-G-T

188988555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45364929-T-C

188988604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45364979-C-T

188988749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365128-A-G

188988749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365128-A-T

188988772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365151-A-G

188988787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365169-G-T

188988788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365170-T-C

188988826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365193-A-G

188988852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365210-C-G

http://identifiers.org/hco/2/GRCh38#188989363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45365702-A-C

188989363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365702-A-T

188989512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365851-T-C

http://identifiers.org/hco/2/GRCh38#188989520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45365859-A-C

188989522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365861-G-A

188989522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365861-G-C

188989538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45365874-A-G

188989827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366369-C-T

188989841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366383-A-G

188989881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366433-T-C

188989881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366433-T-G

http://identifiers.org/hco/2/GRCh38#188990032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45366685-C-A

188990032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366685-C-T

188990035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366688-A-G

188990202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45366869-A-G

188990336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45366999-A-G

188990694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367112-G-A

188990889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367297-T-C

188990896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367304-G-T

188990899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367309-A-G

http://identifiers.org/hco/2/GRCh38#188990945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45367356-C-A

188990945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367356-C-G

188991039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45367628-A-G

188991039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45367628-A-T

188991216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367785-C-T

188991248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367815-T-C

188991279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367846-A-G

188991279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367846-A-T

188991284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367851-T-G

188991370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367941-T-G

http://identifiers.org/hco/2/GRCh38#188991408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45367969-C-A

188991408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45367969-C-T

188991449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368001-T-C

188991463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368015-G-A

188991463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368015-G-C

188991552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368103-T-A

188991552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368103-T-C

188991561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368112-G-A

188991587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368135-T-C

188991644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45368188-A-G

188991674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45368218-A-G

188992298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369373-T-A

188992298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369373-T-C

188992303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369378-A-G

188992320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369392-G-C

188992599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369550-A-G

188992634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369582-C-T

188992965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369793-G-C

188992986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369805-A-G

188993033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369852-T-A

188993044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369866-G-T

188993085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45369991-T-C

188993227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370134-T-C

http://identifiers.org/hco/2/GRCh38#188993274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45370181-A-C

188993274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370181-A-T

188993278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370185-G-A

188993278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370185-G-C

188993335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370239-C-G

188993335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370239-C-T

188993337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370241-G-T

188993408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45370313-A-G

188993565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370413-G-A

188994032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45370671-A-G

188994176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370782-G-A

188994178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45370784-T-C

188994239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45370843-C-T

188994600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45371192-T-C

http://identifiers.org/hco/2/GRCh38#188994675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45371263-C-A

188994675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45371263-C-T

188994947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372023-T-G

188994985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372066-A-G

188994991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372072-A-G

188994993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372074-G-C

188995276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372357-C-T

http://identifiers.org/hco/2/GRCh38#188995534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45372575-C-A

188995534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372575-C-G

188995534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372575-C-T

188995548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372589-C-T

http://identifiers.org/hco/2/GRCh38#188995570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45372611-C-A

188995570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372611-C-T

http://identifiers.org/hco/2/GRCh38#188995882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45372908-C-A

http://identifiers.org/hco/2/GRCh38#188995900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45372926-A-C

188995900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372926-A-G

188995900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372926-A-T

http://identifiers.org/hco/2/GRCh38#188995922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45372951-C-A

188995926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372975-T-C

188995948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45372997-G-A

188995960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45373009-G-C

188996364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45373338-T-G

188996554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45373533-A-G

188996554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45373533-A-T

188997209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45373801-T-A

http://identifiers.org/hco/2/GRCh38#188997377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45373962-C-A

188997377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45373962-C-G

188997377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45373962-C-T

188997463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45374043-A-G

http://identifiers.org/hco/2/GRCh38#188997515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45374094-C-A

188997538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45374117-G-A

188997705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45374300-T-C

188997738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45374333-T-A

188997859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45374496-C-T

188998465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375644-T-A

188998465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375644-T-G

188998518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375695-T-A

188998567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375750-T-C

188998568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375751-G-A

188998861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45375997-T-A

http://identifiers.org/hco/2/GRCh38#188999146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45376256-A-C

188999146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376256-A-G

188999146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376256-A-T

188999222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376339-T-A

188999222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376339-T-C

188999308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45376424-A-T

188999341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45376457-A-T

188999442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376558-T-C

http://identifiers.org/hco/2/GRCh38#188999640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45376919-A-C

188999640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45376919-A-T

http://identifiers.org/hco/2/GRCh38#188999754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45377044-C-A

188999754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377044-C-T

188999758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377048-A-G

188999823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377099-A-G

188999837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45377113-G-A

188999837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45377113-G-T

http://identifiers.org/hco/2/GRCh38#188999962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45377237-A-C

188999962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377237-A-T

http://identifiers.org/hco/2/GRCh38#189001065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45377424-A-C

189001071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377430-G-C

189001338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377679-T-C

http://identifiers.org/hco/2/GRCh38#189001347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45377688-A-C

189001352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377693-G-A

189001375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377716-A-G

http://identifiers.org/hco/2/GRCh38#189001625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45377958-C-A

189001674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45377991-C-T

189001734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378037-T-C

189001822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378117-A-G

189002102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, undefined
orthologous variants: 45378386-G-A

189002312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous_variant, undefined
orthologous variants: 45378533-A-G

189002314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, undefined
orthologous variants: 45378535-C-G

189002336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous_variant, undefined
orthologous variants: 45378557-T-C

189002342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45378563-T-C

http://identifiers.org/hco/2/GRCh38#189002380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45378601-C-A

189002380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378601-C-T

http://identifiers.org/hco/2/GRCh38#189002388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45378609-C-A

189002388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378609-C-T

189002441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378660-T-C

189002469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378687-T-A

189002469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378687-T-G

189002632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378777-T-C

189002664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378804-T-A

http://identifiers.org/hco/2/GRCh38#189002720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45378814-C-A

189002720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378814-C-T

189002724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378818-C-T

189002726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378820-C-T

189002856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378926-T-C

189002913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45378992-A-G

http://identifiers.org/hco/2/GRCh38#189002925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45379004-C-A

189002947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45379026-G-A

189002947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45379026-G-T

189002975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45379054-T-C

189003023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45379102-T-C

http://identifiers.org/hco/2/GRCh38#189003039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45379118-C-A

189003039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45379118-C-G

189003039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45379118-C-T

189003048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45379127-G-A

189003048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45379127-G-C

189003048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45379127-G-T

189003279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45379264-T-A

189003279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45379264-T-C

189003288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45379273-G-A

189003288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45379273-G-T

http://identifiers.org/hco/2/GRCh38#189003339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45379340-C-A

189003446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45379450-T-C

189003486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45379490-T-C

189003519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45379536-T-C

189003519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45379536-T-G

http://identifiers.org/hco/2/GRCh38#189003541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45379557-C-A

189003567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45379583-T-G

189003646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45379699-G-A

189003751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45379807-T-C

189003879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45379930-T-A

189004287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45380328-A-G

189004287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45380328-A-T

189004408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380450-G-A

189004408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380450-G-C

189004408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380450-G-T

189004465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380504-A-G

189004525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380565-A-G

189004526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380566-T-C

http://identifiers.org/hco/2/GRCh38#189004698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45380740-A-C

189004722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380762-T-A

189004827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380858-T-C

189004860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45380891-G-T

189005136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381090-C-T

189005239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381194-A-G

189005287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381225-A-G

189005315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381253-T-C

189005315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381253-T-G

http://identifiers.org/hco/2/GRCh38#189005347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45381280-C-A

189005487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381473-G-A

189005535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381625-G-A

189005535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381625-G-T

189005616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381775-A-G

189005629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381789-T-C

http://identifiers.org/hco/2/GRCh38#189005699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45381856-A-C

189005699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381856-A-T

189005739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381893-G-A

189005739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381893-G-T

189005852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381978-G-A

189005865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45381990-A-G

http://identifiers.org/hco/2/GRCh38#189006005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45382134-C-A

189006005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45382134-C-T

http://identifiers.org/hco/2/GRCh38#189006044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45382182-C-A

http://identifiers.org/hco/2/GRCh38#189006129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45382316-C-A

http://identifiers.org/hco/2/GRCh38#189006383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45382592-C-A

189006383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45382592-C-G

189006383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45382592-C-T

http://identifiers.org/hco/2/GRCh38#189006416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45382625-C-A

189006416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: synonymous variant
orthologous variants: 45382625-C-T

189006423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45382632-G-A

189006468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45382677-C-T

189006508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45382723-T-A

189006514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45382729-G-A

189006514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45382729-G-T

189006848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383037-A-G

189006862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383051-T-C

http://identifiers.org/hco/2/GRCh38#189006894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45383083-C-A

189006894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383083-C-T

189007000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383190-G-A

http://identifiers.org/hco/2/GRCh38#189007071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45383240-C-A

189007071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383240-C-T

http://identifiers.org/hco/2/GRCh38#189007367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45383426-C-A

189007386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383445-G-A

189007386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383445-G-T

189007417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383502-T-C

189007453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383572-A-G

189007470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383589-A-G

189007637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383758-C-T

189007639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383760-T-C

189007714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383798-A-G

189007744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383828-A-G

189007866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383938-A-G

189007867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45383939-C-T

189007909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense variant
orthologous variants: 45383981-A-G

189007975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384047-T-G

189008003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384075-T-C

189008005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384078-T-C

189008007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384080-G-A

189008007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384080-G-T

189008241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: 45384300-A-G

http://identifiers.org/hco/2/GRCh38#189008301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45384359-A-C

http://identifiers.org/hco/2/GRCh38#189008308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45384366-C-A

189008308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384366-C-G

189008327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384384-G-A

189008424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384498-C-T

189008476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384536-C-T

http://identifiers.org/hco/2/GRCh38#189008526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45384585-A-C

189008526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384585-A-G

189008561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384622-T-C

http://identifiers.org/hco/2/GRCh38#189008599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45384717-C-A

189008599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384717-C-G

189008603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384730-T-G

189008612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384739-T-A

189008612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384739-T-C

189008751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384853-T-C

189008751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384853-T-G

189008754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384856-T-G

189008874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384958-G-A

189008874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384958-G-C

189008891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45384975-A-T

189009193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45385274-G-A

189009193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45385274-G-T

189009328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385409-G-C

189009378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385480-A-G

189009603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385757-T-C

189009681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385841-G-C

189009742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385919-G-C

189009836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45385976-G-A

http://identifiers.org/hco/2/GRCh38#189009880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386005-A-C

http://identifiers.org/hco/2/GRCh38#189009928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386057-C-A

189010004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45386116-A-G

http://identifiers.org/hco/2/GRCh38#189010061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386161-C-A

189010061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45386161-C-G

189010090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45386188-A-G

189010090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45386188-A-T

189010166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45386268-G-T

189010206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386308-A-G

189010206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386308-A-T

189010213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386315-T-C

189010224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386326-C-T

189010227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386329-G-A

189010227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386329-G-C

189010227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386329-G-T

189010239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386341-T-A

189010239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386341-T-C

189010239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386341-T-G

189010289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386391-G-A

189010289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386391-G-C

189010385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45386487-T-A

189010446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45386540-G-A

189010457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45386551-G-A

189010668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386816-A-G

http://identifiers.org/hco/2/GRCh38#189010684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386832-C-A

189010684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386832-C-T

189010707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386855-T-G

189010708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45386856-C-T

http://identifiers.org/hco/2/GRCh38#189010716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386864-C-A

189010716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386864-C-G

189010716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386864-C-T

189010725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386873-A-G

189010758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386906-T-C

http://identifiers.org/hco/2/GRCh38#189010767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386915-A-C

189010767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386915-A-G

189010770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45386918-C-G

189010770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386918-C-T

189010801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45386949-G-T

http://identifiers.org/hco/2/GRCh38#189010803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45386951-C-A

189010803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386951-C-T

189010818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386966-G-A

189010818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386966-G-C

189010818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386966-G-T

189010830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45386978-T-C

189011147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387300-A-G

189011147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387300-A-T

189011235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387388-T-C

189011304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387435-A-G

189011307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387438-G-A

http://identifiers.org/hco/2/GRCh38#189011346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45387477-C-A

189011527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387650-A-T

189011532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387655-T-C

189011572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45387695-G-C

189011705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45387838-T-A

189011705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45387838-T-C

189011751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45387884-G-A

189011822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45387952-T-C

189011835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45387965-C-T

189011863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45387993-G-A

189011863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45387993-G-T

189011891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45388021-A-G

http://identifiers.org/hco/2/GRCh38#189011902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45388031-C-A

189011902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45388031-C-T

189011905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45388034-T-A

189011905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45388034-T-C

http://identifiers.org/hco/2/GRCh38#189012110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45388236-C-A

189012110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388236-C-T

189012123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388249-G-T

189012222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388344-T-A

http://identifiers.org/hco/2/GRCh38#189012225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#45388347-C-A

189012258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388380-A-G

189012290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388412-G-T

189012298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388425-T-G

189012365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388494-A-G

189012610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388732-T-A

189012610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388732-T-C

189012653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388776-G-T

189012657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2201
most severe consequence: 3 prime UTR variant
orthologous variants: 45388780-G-A