http://identifiers.org/hco/10/GRCh38#123706219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131607636-C-A

123706219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131607636-C-G

123706235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131607651-G-A

123706235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131607651-G-T

http://identifiers.org/hco/10/GRCh38#123706323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131607749-C-A

123706323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131607749-C-T

123706768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131608178-C-T

123708069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131610279-A-G

123708106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131610315-G-A

123708110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131610319-G-A

123708358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610540-A-T

123708402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610579-T-C

123708519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131610687-G-T

http://identifiers.org/hco/10/GRCh38#123708548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131610723-C-A

123708602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 131610775-G-A

123708626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131610800-T-C

123709989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131611824-G-A

123710025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131611857-T-G

123710273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612075-G-A

123710423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612197-C-T

123710464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612233-G-T

123710529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612272-C-T

123710574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612316-C-T

123710676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612417-G-A

123710676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612417-G-T

123710712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612451-G-T

http://identifiers.org/hco/10/GRCh38#123710713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131612452-C-A

123710713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612452-C-T

123710723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612462-T-C

http://identifiers.org/hco/10/GRCh38#123710751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131612490-A-C

http://identifiers.org/hco/10/GRCh38#123711034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131612598-C-A

123711071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612616-A-G

123711072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612617-A-T

123711073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612618-G-C

123711094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131612639-A-G

123711245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131612776-C-T

123711317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131612854-A-G

123711438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131612972-G-A

123711489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613023-T-C

123711598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613139-G-T

123711623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613164-G-A

123711671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613212-G-A

123711678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613219-T-C

123711679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613220-G-C

123711699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131613241-A-G

http://identifiers.org/hco/10/GRCh38#123712722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131613723-C-A

123712781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131613740-G-T

123712804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131613763-G-T

http://identifiers.org/hco/10/GRCh38#123713044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131613949-A-C

123713091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131613990-G-A

http://identifiers.org/hco/10/GRCh38#123713099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131613998-C-A

123713117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131614016-C-T

http://identifiers.org/hco/10/GRCh38#123713155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131614044-A-C

123713155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131614044-A-G

http://identifiers.org/hco/10/GRCh38#123713204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131614093-C-A

123713242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131614160-T-C

123713269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non coding transcript exon variant
orthologous variants: 131614187-A-G

123717539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131614762-G-A

123717580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131614805-C-T

123717720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131614948-G-C

123718114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131615433-A-G

123718334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131615641-C-T

123721440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131620545-A-G

123721480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131620594-G-T

123721497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131620611-G-T

123722326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131621271-T-A

123723030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131621659-T-C

123723109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131621722-T-G

123724017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626252-T-C

123724041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626275-C-T

123724211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626438-A-G

123724318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626537-T-C

123724333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626561-G-T

123724354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626580-C-T

123724374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626600-G-A

123724450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626676-G-A

123724450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626676-G-C

123724587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131626815-C-G

http://identifiers.org/hco/10/GRCh38#123724607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131626835-C-A

123725570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131627814-G-C

123725598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131627841-A-G

123725839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628068-T-A

123725839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628068-T-C

123725839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628068-T-G

123725874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628104-A-G

123725890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628121-C-T

123726344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628294-G-A

123726392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628342-T-C

123726519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628472-T-A

123726677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628593-G-A

123726833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628748-C-T

123726846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131628761-C-T

123727109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131629002-G-T

123727195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131629097-A-G

123727285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131629189-G-A

123727380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131629253-T-A

123727658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131631703-G-C

123727872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131631932-C-G

123727928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131632004-C-T

123728007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131632089-G-A

123728116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131632191-G-A

123728118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131632193-G-A

http://identifiers.org/hco/10/GRCh38#123728276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131632361-C-A

123728360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131632446-G-A

http://identifiers.org/hco/10/GRCh38#123728554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131632546-C-A

123729432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131633212-C-T

123729636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131633782-T-C

http://identifiers.org/hco/10/GRCh38#123729673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131633823-C-A

123729748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131633922-C-G

123729748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131633922-C-T

123729770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131633940-G-T

http://identifiers.org/hco/10/GRCh38#123743573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#131642720-C-A

123743573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131642720-C-T

123743768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131642910-G-T

123744188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131643244-C-T

123744241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131643265-G-A

123744629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131643471-C-T

123744911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131643697-G-T

123745715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644632-C-T

123745757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644674-C-T

123745762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644679-G-A

123745938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644842-T-C

http://identifiers.org/hco/10/GRCh38#123745971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131644858-C-A

123746022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644900-A-G

http://identifiers.org/hco/10/GRCh38#123746110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131644972-C-A

123746110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131644972-C-T

http://identifiers.org/hco/10/GRCh38#123746115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131644977-C-A

http://identifiers.org/hco/10/GRCh38#123746188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131645051-A-C

123746193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645056-T-C

123746201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645062-G-T

http://identifiers.org/hco/10/GRCh38#123746271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131645136-A-C

123746324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645191-A-G

123746380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645246-A-G

http://identifiers.org/hco/10/GRCh38#123746588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131645447-A-C

123746588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645447-A-G

http://identifiers.org/hco/10/GRCh38#123746624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131645483-A-C

123746624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645483-A-G

123746624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645483-A-T

123746656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645515-A-G

123746662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645521-T-C

123746668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131645527-A-G

http://identifiers.org/hco/10/GRCh38#123746806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131645664-C-A

123746995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131645853-G-A

123747037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131645893-G-A

123747037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131645893-G-C

123747409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131646218-C-T

123747529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131646320-T-C

123747529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131646320-T-G

123750422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131647568-A-G

123750500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131647637-C-G

http://identifiers.org/hco/10/GRCh38#123750538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131647674-A-C

123750542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131647678-T-A

123750682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131647812-C-T

123750927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131648049-G-A

123751541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648239-A-G

123751770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648442-T-C

123751911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648623-C-T

123752187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648873-T-A

123752209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648895-A-T

123752284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131648998-T-C

123752358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131649071-A-G

123754465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649200-G-C

123754573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649297-G-T

123754606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649388-T-C

123754610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649392-T-C

123754809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649585-G-A

http://identifiers.org/hco/10/GRCh38#123754817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131649593-C-A

123754817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649593-C-T

http://identifiers.org/hco/10/GRCh38#123754827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131649603-A-C

123754827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649603-A-G

123754827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649603-A-T

123754878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649653-G-A

123754878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131649653-G-T

http://identifiers.org/hco/10/GRCh38#123757197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131650704-C-A

123757197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131650704-C-T

123757249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131650754-C-T

123757275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131650780-C-T

123757276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131650781-A-T

123757324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131650829-T-C

123757390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131650892-A-T

123757427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131650915-G-A

123757427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131650915-G-T

123757701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651030-T-G

123757972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651304-G-A

123758065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651371-C-T

123758096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651403-A-G

http://identifiers.org/hco/10/GRCh38#123758193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131651486-C-A

123758257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651532-T-C

123758287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651557-G-A

123758357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651614-A-G

123758557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131651833-A-G

123758763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652137-C-G

123758793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652175-C-T

123758885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652267-A-G

123759304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652806-A-G

123759392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652978-T-G

123759404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652990-T-C

123759404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131652990-T-G

123759460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653046-G-T

123759638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653220-C-G

123759664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653239-T-A

http://identifiers.org/hco/10/GRCh38#123759761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131653277-C-A

123759761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653277-C-T

123759811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653325-G-A

123759849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653358-C-T

123759896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653404-C-G

123760062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653547-T-A

123760158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653652-C-T

123760172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131653668-G-A

123760713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131654561-C-T

123760815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131654640-C-T

123761172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131654950-G-C

123761218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131654968-G-A

123761252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131654993-G-A

123761291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655025-G-C

http://identifiers.org/hco/10/GRCh38#123761385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131655107-C-A

123761718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655370-G-A

123761718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655370-G-T

123761723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655375-T-C

123761723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655375-T-G

123761730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655382-G-A

123761730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131655382-G-T

123761905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131656493-C-T

123761933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131656521-C-T

123761946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131656534-C-G

http://identifiers.org/hco/10/GRCh38#123761996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131656584-C-A

123762056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131656644-C-T

123762143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131656731-T-C

123762148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131656736-C-G

123762148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131656736-C-T

123762257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131656824-G-C

123762257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131656824-G-T

123762304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131656871-T-C

123766895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659279-G-A

123766895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659279-G-T

123766901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659293-T-C

123766979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131659369-A-T

123767068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131659458-G-A

123767071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131659461-T-A

http://identifiers.org/hco/10/GRCh38#123767081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131659471-A-C

http://identifiers.org/hco/10/GRCh38#123767144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131659534-C-A

123767144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131659534-C-G

123767184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659574-A-G

http://identifiers.org/hco/10/GRCh38#123767200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131659590-C-A

123767200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659590-C-G

123767200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659590-C-T

123767201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659591-G-A

123767201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659591-G-C

123767201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659591-G-T

123767232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659612-C-G

123767232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659612-C-T

http://identifiers.org/hco/10/GRCh38#123767240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131659620-C-A

123767240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131659620-C-T

123767333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660134-G-A

123767437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660229-C-T

123767510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660330-C-T

123767528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660348-A-G

123767543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660384-T-G

123767626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660542-T-C

123767708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660621-T-C

123767853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660739-T-G

123767881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660767-G-A

123767980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660840-G-A

123768056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131660921-C-T

123768360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661217-G-C

123768360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661217-G-T

123768395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661252-A-G

http://identifiers.org/hco/10/GRCh38#123768413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131661299-A-C

123768413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661299-A-G

123768413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661299-A-T

123768420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661306-T-C

123768420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661306-T-G

123768446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661338-T-C

123768589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131661526-C-T

123768613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131661550-A-G

123768637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131661574-C-T

123768664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131661601-C-T

123768670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131661607-G-A

123768740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661675-G-A

123768740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661675-G-C

123768740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661675-G-T

123768765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661698-A-G

123768765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661698-A-T

123768817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661733-A-G

http://identifiers.org/hco/10/GRCh38#123768874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131661782-A-C

123768874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661782-A-G

123768879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661787-G-A

123768879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661787-G-T

http://identifiers.org/hco/10/GRCh38#123768990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131661890-C-A

123769099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131661987-A-G

http://identifiers.org/hco/10/GRCh38#123769126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131662003-C-A

123769133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131662010-T-C

123769904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131662669-A-G

123769904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131662669-A-T

123770570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131663005-T-C

123770623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131663062-C-G

123770682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131663117-T-C

123770967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131663847-G-C

http://identifiers.org/hco/10/GRCh38#123771133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131664002-C-A

123771133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664002-C-G

123771133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664002-C-T

http://identifiers.org/hco/10/GRCh38#123771148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131664020-C-A

123771148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664020-C-T

http://identifiers.org/hco/10/GRCh38#123771168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131664040-C-A

123771168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664040-C-T

123771277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664137-C-T

123771298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664157-C-T

http://identifiers.org/hco/10/GRCh38#123773251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131664750-A-C

123773266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664773-G-A

123773276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131664783-C-G

123773732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665068-G-C

123773957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665272-G-A

123775262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665625-A-G

123775279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665641-T-A

123775279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665641-T-C

http://identifiers.org/hco/10/GRCh38#123775458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131665804-C-A

123775458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665804-C-T

123775531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665848-C-T

123775550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665866-G-A

123775592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131665909-C-T

http://identifiers.org/hco/10/GRCh38#123775627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131665946-A-C

123775826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131666143-T-C

123775826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131666143-T-G

123775947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131666277-A-G

123776803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131667851-C-T

123776820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131667868-T-A

123776875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131667912-A-T

123776909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131667946-T-C

123776938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131667968-G-T

http://identifiers.org/hco/10/GRCh38#123777009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668012-C-A

123777009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668012-C-G

123777020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668023-G-T

123777081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668108-T-C

123777115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 131668152-T-C

http://identifiers.org/hco/10/GRCh38#123777192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668234-C-A

123777194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668236-G-T

http://identifiers.org/hco/10/GRCh38#123777200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668242-C-A

123777242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668283-G-T

123777291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668325-A-G

123777339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668374-G-A

123777368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668403-C-T

123777472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668525-T-C

123777586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668610-T-C

123777591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668615-A-G

http://identifiers.org/hco/10/GRCh38#123777592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668616-C-A

123777665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668671-G-A

123777665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668671-G-T

123777674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668680-T-C

123777703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668718-G-A

123777703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668718-G-C

http://identifiers.org/hco/10/GRCh38#123777705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668720-C-A

http://identifiers.org/hco/10/GRCh38#123777719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668734-C-A

http://identifiers.org/hco/10/GRCh38#123777748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668763-C-A

123777748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668763-C-T

http://identifiers.org/hco/10/GRCh38#123777755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668770-C-A

123777755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668770-C-T

http://identifiers.org/hco/10/GRCh38#123777776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131668792-C-A

123777776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131668792-C-T

123777857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668863-T-A

123777857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668863-T-C

123777878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668879-C-T

123777904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668905-G-A

123777904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131668905-G-C

123778197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669206-T-A

123778388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669392-C-T

123778480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669472-G-T

123778595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669585-T-C

123778596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669586-G-A

123778629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669611-G-C

123778817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669788-T-C

123778856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131669827-G-A

123779056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131670022-C-T

123779065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131670031-A-G

123779184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131670147-T-G

123779775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672242-T-C

123779775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672242-T-G

123779802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672267-T-C

123780097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672480-G-T

123780119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672502-G-A

123780119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672502-G-C

123780119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672502-G-T

123780120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672503-C-T

123780147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672527-C-T

123780148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672528-T-C

123780149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672529-T-C

123780261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 131672640-G-T

123780317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672690-T-C

123780318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672691-T-C

http://identifiers.org/hco/10/GRCh38#123780323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131672696-A-C

123780347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672717-G-A

123780347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672717-G-T

http://identifiers.org/hco/10/GRCh38#123780351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131672721-C-A

123780351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672721-C-T

123780356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672726-T-C

http://identifiers.org/hco/10/GRCh38#123780370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131672741-C-A

123780370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672741-C-T

123780379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672751-A-G

123780406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672779-G-A

123780462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131672834-G-A

123780995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673196-C-T

123781258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673822-T-A

123781332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673888-T-C

123781335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673891-A-G

http://identifiers.org/hco/10/GRCh38#123781355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131673910-C-A

123781434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673984-G-A

123781443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673993-G-A

123781443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131673993-G-T

http://identifiers.org/hco/10/GRCh38#123781477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131674053-A-C

123781743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131674255-T-C

123781944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131674415-C-T

http://identifiers.org/hco/10/GRCh38#123782081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131674530-C-A

123782081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131674530-C-T

http://identifiers.org/hco/10/GRCh38#123782293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131674719-C-A

123782433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131674861-A-G

123782434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131674862-T-C

123783572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131676048-G-A

123783638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131676105-G-A

123783638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131676105-G-T

123783807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131676265-C-T

123783984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131676459-T-A

123795746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131678640-C-G

123795859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131678724-C-T

123795945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131678807-G-C

123796603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131679417-G-A

123796605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131679419-T-A

123796611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131679425-A-T

123796664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131679478-A-T

http://identifiers.org/hco/10/GRCh38#123796913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131679722-C-A

123796919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131679728-G-A

http://identifiers.org/hco/10/GRCh38#123797278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131680060-A-C

123797986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131680512-G-A

123798022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131680548-A-G

123798481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131680906-T-G

123798969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681638-G-A

123798969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681638-G-C

123798969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681638-G-T

123798971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681640-G-T

http://identifiers.org/hco/10/GRCh38#123798979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131681648-C-A

123798979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681648-C-T

123798989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681658-G-T

123799014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681683-G-A

123799014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681683-G-T

123799222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681877-T-C

http://identifiers.org/hco/10/GRCh38#123799250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131681905-C-A

123799250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681905-C-T

123799282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681938-A-G

123799307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681957-G-A

123799307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681957-G-T

http://identifiers.org/hco/10/GRCh38#123799309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131681959-C-A

123799311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131681961-A-G

123800447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682617-G-A

123800470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682637-T-C

123800525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682690-C-T

123800541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682701-G-A

123800543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682703-C-T

123800719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131682868-T-A

123807804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131683933-T-C

123807804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131683933-T-G

123807969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684080-G-A

123808250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684297-T-C

123808383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684413-C-T

123808545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684557-A-T

123808633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684641-T-C

123808788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131684801-G-A

123813603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131687291-C-G

123813603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131687291-C-T

http://identifiers.org/hco/10/GRCh38#123813605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131687293-C-A

123821152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690142-A-G

123821313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690316-C-T

123821474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690475-T-A

123821631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690625-G-A

123821724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690739-C-T

123821894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131690873-A-T

123822113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131691072-T-G

123823861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693088-T-C

123823996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693217-C-T

123824107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693352-G-C

123824193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693444-G-A

123824244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693491-A-T

123824411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693666-C-T

123824685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131693909-C-T

123830265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131695752-T-C

123830740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131696443-G-A

123830740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131696443-G-C

123831088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131696732-T-C

123831155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131696795-C-T

123831191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131696830-A-G

123831592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131697225-G-T

http://identifiers.org/hco/10/GRCh38#123831732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131697348-C-A

123833447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131698112-T-C

123833997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131698452-A-G

123834161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131698973-G-A

123834161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131698973-G-C

123834544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699302-G-T

123834551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699309-G-T

123834559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699317-G-A

http://identifiers.org/hco/10/GRCh38#123834976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131699619-C-A

http://identifiers.org/hco/10/GRCh38#123834977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131699620-A-C

123835123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699714-C-T

123835177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699756-G-A

123835177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699756-G-C

123835177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699756-G-T

http://identifiers.org/hco/10/GRCh38#123835255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131699832-C-A

http://identifiers.org/hco/10/GRCh38#123835266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131699843-C-A

123835284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699860-G-A

123835324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131699899-G-A

123835843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700460-A-G

123835938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700559-A-G

123835969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700581-G-A

123835972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700584-C-T

123835975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700587-C-T

123835978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700590-G-A

123835978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700590-G-C

123836003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700618-C-T

123836095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700698-G-A

http://identifiers.org/hco/10/GRCh38#123836185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131700783-C-A

http://identifiers.org/hco/10/GRCh38#123836202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131700800-C-A

123836431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131700956-C-T

http://identifiers.org/hco/10/GRCh38#123836584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131701108-C-A

123836681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131701205-G-A

123836929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131701278-A-T

123837138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131701454-A-G

http://identifiers.org/hco/10/GRCh38#123837145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131701461-C-A

http://identifiers.org/hco/10/GRCh38#123837260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131701575-C-A

123837260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131701575-C-T

123837474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131701807-T-C

123838159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131702409-A-G

http://identifiers.org/hco/10/GRCh38#123838976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131703237-A-C

123839035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131703296-T-C

123839275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131703603-C-T

123839402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131703725-C-T

http://identifiers.org/hco/10/GRCh38#123839662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131703933-A-C

123840320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131704672-A-G

123840628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131704984-G-A

123840731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131705078-C-T

123840762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131705106-T-C

123840762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131705106-T-G

123841424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131706554-T-G

123841473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131706612-C-T

123841489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131706628-T-C

123841506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131706644-C-T

123841750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707486-A-G

123841789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707522-C-T

123841830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707563-T-A

http://identifiers.org/hco/10/GRCh38#123841874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131707601-A-C

123841955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707685-T-A

123842014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707745-C-T

123842048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707779-T-C

123842062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707798-C-T

123842070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707809-G-A

123842070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707809-G-T

123842198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707898-G-A

123842198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707898-G-T

123842263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707946-T-A

123842263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131707946-T-C

123842426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131708089-C-G

123842639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131708261-C-T

123842737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131708341-T-G

123842856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131708806-T-C

123843017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131708953-T-C

123843062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131708999-T-C

123843291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131709085-T-G

123843747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131709701-T-A

123843749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131709703-T-C

123844102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131713878-T-C

123844363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131714313-G-A

123844729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131714640-G-A

123844742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131714641-G-A

123846735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131718408-G-A

123846821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131718472-A-G

123847021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131718636-A-G

123847773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131719313-G-T

123847904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131719423-T-C

123847915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131719434-T-C

123849252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131720629-T-C

123849364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131720741-C-T

123849372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131720749-C-T

http://identifiers.org/hco/10/GRCh38#123849434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131720805-A-C

123849434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131720805-A-G

123849434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131720805-A-T

123855094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131721671-G-A

123855206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131721782-G-T

http://identifiers.org/hco/10/GRCh38#123855269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131721847-A-C

123855461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131722053-G-T

123855549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131722181-T-A

123855549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131722181-T-G

123856005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131722701-G-A

123856076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131722757-G-A

123856295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131723433-G-A

123856480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131723589-G-T

123856526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724522-G-A

123857031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724666-T-C

123857069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724701-C-T

123857071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724703-T-C

123857094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724733-T-A

123857163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724797-T-C

123857296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724925-A-G

123857319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131724940-A-T

123858425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131726606-G-C

123858498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131726669-T-C

123858517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131726688-G-A

123858654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131726825-G-C

123858686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131726855-T-C

123859076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131727193-G-A

http://identifiers.org/hco/10/GRCh38#123859096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#131727213-C-A

123859104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131727221-G-T

123859369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131727491-G-C

123859370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131727492-C-T

123859391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131727514-A-G

123859826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131728407-G-T

123859836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131728417-G-A

123859836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131728417-G-T

123862572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730044-A-T

123862609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730076-G-A

123862609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730076-G-T

123862617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131730084-G-A

123862635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131730102-A-G

123862771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730230-G-A

123862771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730230-G-T

123862772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730231-A-G

123862784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730243-T-C

123862928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131730402-G-C

123863510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732083-G-A

123863510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732083-G-C

123863558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732133-T-C

123863558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732133-T-G

http://identifiers.org/hco/10/GRCh38#123863617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131732192-C-A

123863638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732219-G-A

123863695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732271-G-A

123863805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732354-G-A

123863913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131732471-C-T

123864377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732869-G-A

123864394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732885-G-A

123864411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131732902-T-C

http://identifiers.org/hco/10/GRCh38#123864475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131732967-C-A

123864669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131733130-G-A

http://identifiers.org/hco/10/GRCh38#123864955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131733371-C-A

123864955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131733371-C-T

123865449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131733861-G-A

123867245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131734962-T-G

123867614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735178-C-T

123867898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735331-C-G

123868031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735387-T-A

123868209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735558-G-A

123868209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735558-G-C

123868556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735840-G-C

123868645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131735912-G-C

123868852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131736068-C-T

123869094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131736282-T-C

123869261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131736673-C-T

123869456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131736833-A-G

123869684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131737040-C-G

123869684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131737040-C-T

123870033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131737993-G-A

123870308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131738274-A-G

123870363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131738334-G-A

http://identifiers.org/hco/10/GRCh38#123870432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131738385-C-A

123870432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131738385-C-T

123870882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131738873-G-T

123870918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131738908-T-A

http://identifiers.org/hco/10/GRCh38#123870988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131738979-C-A

123871182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739164-C-T

123871194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739176-C-T

123871246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739222-G-A

123871314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739276-T-C

123871314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739276-T-G

123871368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739334-T-A

123871471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739435-T-C

123871538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739479-C-T

123871702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739623-A-T

123871721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739642-T-C

123871780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131739701-T-G

http://identifiers.org/hco/10/GRCh38#123872104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131740012-A-C

123872200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131740084-T-A

123872210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131740094-C-T

123877617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742272-C-T

123877628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742282-T-C

123877667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742320-C-T

http://identifiers.org/hco/10/GRCh38#123877793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131742444-C-A

123877810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742461-C-G

http://identifiers.org/hco/10/GRCh38#123877825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131742475-C-A

123878179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742698-A-G

http://identifiers.org/hco/10/GRCh38#123878190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131742709-A-C

123878319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742818-T-G

123878399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131742899-G-C

http://identifiers.org/hco/10/GRCh38#123878409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131742909-C-A

123878513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131743050-G-A

123878535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131743095-G-T

123878537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131743097-G-T

123879147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131744061-G-A

123879860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745050-C-T

123879894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745098-A-G

123879955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745160-G-C

123880000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745200-G-C

123880078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745274-T-C

123880078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745274-T-G

123880079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745275-A-G

123880079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745275-A-T

http://identifiers.org/hco/10/GRCh38#123880092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131745286-C-A

123880092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745286-C-T

http://identifiers.org/hco/10/GRCh38#123880129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131745323-C-A

123880129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745323-C-T

123880145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745339-T-C

123880145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745339-T-G

123880251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131745437-A-G

123880353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745546-A-T

123880367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745560-G-T

http://identifiers.org/hco/10/GRCh38#123880398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131745585-C-A

123880443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745624-G-A

123880443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745624-G-C

123880443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745624-G-T

123880501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745670-G-A

123880622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745718-G-A

123880622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745718-G-T

123880623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745719-A-T

123880732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745760-G-A

123881032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745881-G-C

123881069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745904-C-T

123881136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131745965-T-C

http://identifiers.org/hco/10/GRCh38#123881226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131746009-C-A

123881265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131746022-T-A

123881265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131746022-T-C

123881268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131746025-C-T

123883813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747028-T-C

123883889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747103-G-T

123883921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747135-A-G

123884096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747316-G-A

123884137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747360-G-A

123884158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747381-C-T

123884192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131747416-T-C

http://identifiers.org/hco/10/GRCh38#123884225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131747450-C-A

123884784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749157-T-G

123884995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749537-G-A

123885112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749678-T-C

123885195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749768-A-G

123885216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749789-G-A

123885313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749848-C-T

123885402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131749927-C-T

123885840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131750356-C-T

123885902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131750421-A-T

http://identifiers.org/hco/10/GRCh38#123885992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131750510-C-A

123885992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131750510-C-G

123885992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131750510-C-T

123886142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131750652-A-G

123886777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131751305-G-C

123886777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131751305-G-T

http://identifiers.org/hco/10/GRCh38#123886951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131751560-C-A

http://identifiers.org/hco/10/GRCh38#123887018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131751622-C-A

123887080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131751676-C-T

123887123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131751708-T-G

123887915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131752350-A-G

123888061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753230-C-G

http://identifiers.org/hco/10/GRCh38#123888102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131753258-C-A

123888102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753258-C-T

123888268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753417-C-G

123888300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753449-T-C

123888522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753650-G-C

123888618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131753742-A-G

http://identifiers.org/hco/10/GRCh38#123888635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131753755-C-A

123888847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754017-C-T

123888916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754078-C-T

123888950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754088-G-A

123889281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754344-A-G

123889409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754445-C-T

123889416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754452-C-T

http://identifiers.org/hco/10/GRCh38#123889456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131754489-A-C

123889456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754489-A-T

123889478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754500-G-T

http://identifiers.org/hco/10/GRCh38#123889484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131754506-A-C

123889484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754506-A-G

123889484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754506-A-T

123890076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754880-C-T

123890203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131754974-A-T

123890268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755041-A-T

123890442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755181-C-T

123890509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755238-T-A

123890509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755238-T-C

http://identifiers.org/hco/10/GRCh38#123891210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131755882-C-A

123891210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755882-C-G

123891210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755882-C-T

123891240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755913-G-A

123891240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755913-G-T

123891333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755997-G-A

123891333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131755997-G-T

123891411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131756070-G-A

123891411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131756070-G-C

123891411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131756070-G-T

http://identifiers.org/hco/10/GRCh38#123891429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756088-C-A

123891429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131756088-C-T

http://identifiers.org/hco/10/GRCh38#123891461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756132-C-A

123891461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756132-C-T

123891478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756149-A-T

123891479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756150-G-T

http://identifiers.org/hco/10/GRCh38#123891521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756198-A-C

123891521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756198-A-G

123891521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756198-A-T

123891527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756204-G-A

123891527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131756204-G-T

http://identifiers.org/hco/10/GRCh38#123891612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756289-C-A

http://identifiers.org/hco/10/GRCh38#123891672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756355-C-A

123891672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756355-C-T

http://identifiers.org/hco/10/GRCh38#123891723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131756405-C-A

123891723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756405-C-T

123891732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756414-T-A

123891732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756414-T-C

123891732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756414-T-G

123891734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756416-G-A

123891734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131756416-G-T

123891818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131756474-C-G

123891818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131756474-C-T

123892042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131756676-G-A

123892275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131756813-G-A

123892441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131756972-C-T

123892494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757038-A-G

123892509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757057-G-A

123892509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757057-G-C

123892601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757130-C-T

http://identifiers.org/hco/10/GRCh38#123892639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131757157-A-C

123892745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757261-G-A

http://identifiers.org/hco/10/GRCh38#123893206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131757587-C-A

123893206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757587-C-T

123893522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757869-G-A

123893568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131757913-C-T

http://identifiers.org/hco/10/GRCh38#123893668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131758008-A-C

123893668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131758008-A-G

123893687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131758026-C-T

http://identifiers.org/hco/10/GRCh38#123893864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131758211-C-A

123893881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131758230-G-A

http://identifiers.org/hco/10/GRCh38#123894297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131758567-A-C

123894517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131758766-G-A

123894547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131758795-G-T

123894590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131758834-T-C

123895428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131759574-C-T

123895615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131759763-T-A

123895767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131759919-G-A

123896300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131760418-A-G

123896300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131760418-A-T

123896604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131760720-T-C

123896703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131760807-A-G

123900938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761211-T-C

123901041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761325-G-A

123901098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761382-C-T

123901194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761465-C-T

123901282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761903-G-A

123901286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761907-C-T

123901335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131761947-T-G

123902225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131762987-C-T

123902240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131762999-C-T

123902284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763035-A-T

123902286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763037-T-G

123902442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763174-T-C

123902442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763174-T-G

123903529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763335-G-A

123903529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763335-G-T

123903912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763679-G-A

123903970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763738-G-A

123904176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131763945-G-A

http://identifiers.org/hco/10/GRCh38#123904178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131763947-A-C

123904322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131764073-C-T

123904327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131764078-G-A

123904639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765325-G-A

123904639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765325-G-T

123904709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765395-C-T

123904895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131765520-G-A

123904895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131765520-G-T

123905033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765658-G-A

http://identifiers.org/hco/10/GRCh38#123905142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131765723-C-A

123905175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765754-G-A

123905321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765902-G-A

123905397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765971-T-C

123905413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131765987-C-T

123905998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131767702-C-T

http://identifiers.org/hco/10/GRCh38#123906139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131767829-A-C

123906139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131767829-A-G

123906143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131767833-C-T

123906228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131767908-G-A

123906397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131768047-T-G

123906440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131768089-G-A

123906440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131768089-G-C

123906630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131768239-T-G

http://identifiers.org/hco/10/GRCh38#123906673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131768283-C-A

123906707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131768317-T-C

123907084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131768611-T-C

123907253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131768769-A-G

123907544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769078-A-G

123907554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769088-A-T

123907702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769494-T-C

123907749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769541-G-A

123907838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769626-G-A

123907838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769626-G-C

123907929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769724-G-A

123907929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769724-G-T

123908166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769929-G-A

123908178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131769941-T-C

123908652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770323-G-A

123908656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770327-C-T

123908768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770411-A-T

123908871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770485-A-G

123908878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770492-A-G

123908911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770525-T-C

123908938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131770550-T-C

123909032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131770657-C-G

123909032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131770657-C-T

http://identifiers.org/hco/10/GRCh38#123909282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131771155-C-A

123909282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771155-C-T

123909398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771263-A-G

123909752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771623-A-G

123909770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771655-C-T

123909777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771662-G-A

123910877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771876-G-A

123910986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131771957-C-T

123911073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772035-T-A

123911073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772035-T-C

123911195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772156-T-C

123911396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772312-A-T

123911410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772326-C-G

123911426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772341-G-A

123911564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772395-C-T

http://identifiers.org/hco/10/GRCh38#123911578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131772409-A-C

123911578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772409-A-G

123911594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772428-C-T

123911626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772456-A-G

123911650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772480-A-G

123911694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772526-A-G

123911727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772564-C-G

123911739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131772576-A-G

123913093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131773463-C-T

123913331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131773703-G-T

http://identifiers.org/hco/10/GRCh38#123913388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131773759-C-A

123913443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131773814-G-A

123913485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131773858-G-T

123913605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131773982-G-T

123913634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774011-T-A

123913634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774011-T-G

123913649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774026-G-A

123913649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774026-G-C

http://identifiers.org/hco/10/GRCh38#123913702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774077-C-A

123913702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774077-C-T

123913703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774078-G-C

123913705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774080-G-A

123913705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774080-G-T

123913733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 131774111-G-A

123913839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774217-T-C

123913844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774222-C-T

123913866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774244-C-T

123913903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774273-G-A

123913936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774306-C-T

123913940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774310-A-T

http://identifiers.org/hco/10/GRCh38#123913963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774333-C-A

123913969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774339-G-A

123913969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774339-G-T

123913977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774349-G-C

http://identifiers.org/hco/10/GRCh38#123913991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774363-C-A

123913991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774363-C-G

123913991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774363-C-T

http://identifiers.org/hco/10/GRCh38#123913992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774364-C-A

123913992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774364-C-T

123914000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774365-T-A

http://identifiers.org/hco/10/GRCh38#123914018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774383-C-A

123914018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774383-C-T

http://identifiers.org/hco/10/GRCh38#123914086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774438-C-A

123914086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774438-C-T

123914092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131774445-G-T

123914187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131774555-A-G

http://identifiers.org/hco/10/GRCh38#123914248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774609-C-A

http://identifiers.org/hco/10/GRCh38#123914298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131774660-A-C

123915955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131775449-C-T

123916186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131775663-T-G

123916304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131775754-G-C

123916362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131775802-G-C

http://identifiers.org/hco/10/GRCh38#123917033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131776311-C-A

123917116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131776379-T-C

123917183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131776445-C-T

http://identifiers.org/hco/10/GRCh38#123917365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131776624-C-A

123917559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131776790-G-A

123917737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131776952-G-C

123917897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131777063-G-A

http://identifiers.org/hco/10/GRCh38#123918136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131777266-A-C

123918563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131777880-G-T

http://identifiers.org/hco/10/GRCh38#123920400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131778454-C-A

123921120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131778775-T-C

123921408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779057-T-C

123921547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779166-G-T

123921799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779394-G-A

123921906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779488-A-G

123921970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779515-A-G

123922046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779580-G-A

123922296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131779833-G-T

123925293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131785881-G-A

123925293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131785881-G-T

123925484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131786077-A-G

http://identifiers.org/hco/10/GRCh38#123925746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131786297-A-C

123925805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131786356-C-T

123925847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131786400-T-C

123925987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131786536-T-C

123928472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787568-T-A

123928492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787588-T-C

123928588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787634-G-A

123928588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787634-G-T

123928631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787677-T-C

123928798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787838-C-T

123928814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787854-G-T

123928945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131787977-G-A

123928970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788009-G-A

123929031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788061-C-T

123929122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788136-G-T

123929128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788142-A-T

123929220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788212-G-A

123929221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788213-G-C

123929221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788213-G-T

123929257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788245-T-G

123929275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788265-C-T

123929362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788371-A-T

123929402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788411-T-C

123929403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788412-G-A

123929405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788414-C-T

http://identifiers.org/hco/10/GRCh38#123929691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131788612-A-C

123929913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788711-G-A

123929958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788750-T-C

123929989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788784-G-A

123930019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131788814-G-A

http://identifiers.org/hco/10/GRCh38#123930121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131788920-A-C

123930311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789067-G-A

123930311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789067-G-T

123930312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789068-C-T

123930321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789077-C-G

123930464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789202-A-G

123930600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789324-A-G

123930713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789420-C-T

123930745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789475-G-A

http://identifiers.org/hco/10/GRCh38#123930877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131789602-A-C

http://identifiers.org/hco/10/GRCh38#123930887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131789612-A-C

123930960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789662-C-T

123931135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131789817-C-T

http://identifiers.org/hco/10/GRCh38#123934675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131791004-C-A

123934675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791004-C-T

123934767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791114-C-T

123935024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791390-T-G

http://identifiers.org/hco/10/GRCh38#123935029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131791395-C-A

123935029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791395-C-T

123935059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791427-G-A

123935110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791479-T-C

123935337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131791681-G-A

123935477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792426-A-G

123935547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792490-G-C

123935601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792537-G-T

123935645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131792578-G-A

123936083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793489-C-T

123936092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793498-C-G

123936182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793594-C-T

123936190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793602-G-A

http://identifiers.org/hco/10/GRCh38#123936241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131793652-C-A

123936389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793771-G-C

123936406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793788-T-C

123936407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793789-A-G

123936570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131793965-C-T

http://identifiers.org/hco/10/GRCh38#123936652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131794047-C-A

123936757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794121-C-T

http://identifiers.org/hco/10/GRCh38#123936761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131794125-A-C

123936761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794125-A-G

http://identifiers.org/hco/10/GRCh38#123936788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131794154-C-A

123936843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794207-T-G

123936868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794232-C-G

123937042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794386-A-G

123938073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794716-T-C

123938151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794792-C-T

123938156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794797-T-C

123938247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794870-C-T

123938363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131794981-C-T

http://identifiers.org/hco/10/GRCh38#123938383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131795002-C-A

123938383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795002-C-T

123938521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795098-T-C

123938810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795322-C-T

123939178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795615-T-C

123939330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795755-G-T

123939385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795814-G-T

123939390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795819-G-A

123939390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795819-G-T

123939506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131795927-A-G

123939529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 131795950-A-G

123939544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795968-G-A

123939544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131795968-G-T

http://identifiers.org/hco/10/GRCh38#123939612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131796023-C-A

123939613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796024-T-A

123939613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796024-T-C

123939681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796075-G-A

123939736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796131-C-T

123939841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796253-C-G

123939907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796309-C-G

123939986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796383-A-G

123940055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796442-G-T

http://identifiers.org/hco/10/GRCh38#123940073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131796459-C-A

123940073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796459-C-T

123940079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796465-G-A

123940079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796465-G-T

123940146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796515-C-G

123940146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131796515-C-T

123940157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796526-G-A

123940157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796526-G-T

123940207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796565-G-T

http://identifiers.org/hco/10/GRCh38#123940211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#131796569-C-A

123940211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796569-C-T

123940217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796575-C-G

123940217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796575-C-T

123940232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796591-C-T

123940251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131796609-C-T

123940364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron variant
orthologous variants: 131796639-T-C

123940367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron variant
orthologous variants: 131796642-C-G

123940530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26977
most severe consequence: intron variant
orthologous variants: 131796726-C-T