http://identifiers.org/hco/8/GRCh38#43140613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#26466524-A-C

43140613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 26466524-A-G

43140613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 26466524-A-T

43140692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466441-G-A

43140692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466441-G-C

43140692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466441-G-T

43140696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466440-G-A

43140696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466440-G-C

43140696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466440-G-T

43140698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466438-G-A

43140698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26466438-G-T

http://identifiers.org/hco/8/GRCh38#43140714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#26466422-C-A

43140714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26466422-C-T

43142844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26465755-A-G

43142876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26465739-C-T

http://identifiers.org/hco/8/GRCh38#43143191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26465300-A-C

43143231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26465265-C-T

43143232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26465264-T-G

43143459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26465066-G-A

43146177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26464303-T-G

43146263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26464228-T-A

http://identifiers.org/hco/8/GRCh38#43146390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26463489-C-A

43146469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463420-T-C

43146643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463250-T-C

43146647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463246-C-T

43146678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463215-T-G

43146807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463121-G-A

43146813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463115-G-C

http://identifiers.org/hco/8/GRCh38#43146817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26463110-C-A

43146817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463110-C-T

http://identifiers.org/hco/8/GRCh38#43146818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26463109-C-A

http://identifiers.org/hco/8/GRCh38#43146861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26463064-C-A

43146861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463064-C-T

43146862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463063-A-G

43146862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463063-A-T

43146925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26463013-T-A

43147049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 26462882-G-T

43147068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26462863-G-A

43147068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26462863-G-T

43147107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26462804-T-C

43147198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26462718-G-T

43147220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26462697-G-A

http://identifiers.org/hco/8/GRCh38#43158518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26461788-C-A

43158530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461775-G-A

43158593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26461710-G-A

43158593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26461710-G-T

43158605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 26461698-C-T

http://identifiers.org/hco/8/GRCh38#43158688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26461615-C-A

43158701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26461602-G-A

43158726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461579-T-A

http://identifiers.org/hco/8/GRCh38#43158825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26461422-C-A

43158825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461422-C-T

43158831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461416-A-G

http://identifiers.org/hco/8/GRCh38#43158832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26461415-C-A

43158832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461415-C-T

43158843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461404-C-G

43158867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461300-C-T

43159012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26461105-C-G

43159012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26461105-C-T

43159041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26461076-C-T

43159060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461056-C-G

43159060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461056-C-T

http://identifiers.org/hco/8/GRCh38#43159124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26461003-C-A

43159124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26461003-C-T

http://identifiers.org/hco/8/GRCh38#43159229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26460959-A-C

43159599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460807-T-C

43159629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460780-T-C

43159730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460698-G-A

43159741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460683-G-T

http://identifiers.org/hco/8/GRCh38#43159816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26460618-C-A

43159904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460537-G-A

43159989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26460468-A-G

43160939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458979-T-G

43161304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458619-G-A

43161304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458619-G-T

http://identifiers.org/hco/8/GRCh38#43161316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26458581-C-A

43161316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458581-C-T

43161340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458558-T-C

43161340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458558-T-G

43161369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458523-A-G

43161405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458489-T-G

43161462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26458434-G-A

43161501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 26458395-T-A

43161501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26458395-T-G

43161548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458349-T-C

http://identifiers.org/hco/8/GRCh38#43161585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26458313-C-A

43161585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458313-C-T

http://identifiers.org/hco/8/GRCh38#43161593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26458305-C-A

43161612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458238-A-G

43161633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458217-T-C

http://identifiers.org/hco/8/GRCh38#43161639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26458210-C-A

43161732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458130-T-A

43161819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458062-A-G

43161873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26458008-C-G

43161969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26457923-C-G

43162422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26457197-G-A

43162545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26457077-C-T

43167809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26455396-G-T

43168824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26455174-T-G

43168852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26455146-A-G

43168892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26455112-C-T

43169078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454986-A-G

http://identifiers.org/hco/8/GRCh38#43169079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26454985-A-C

43169113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454956-A-G

43169114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454955-A-G

43169161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454901-A-G

43169161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454901-A-T

43169162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454900-T-C

43169163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454899-T-A

43169163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454899-T-C

43169180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26454882-G-A

43169180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26454882-G-T

43169202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26454860-A-G

43169260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454802-T-A

43169260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454802-T-C

43169302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454760-T-A

http://identifiers.org/hco/8/GRCh38#43169315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26454746-C-A

43169350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454705-G-A

43169350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454705-G-T

43169360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26454695-A-G

43170534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453536-A-G

43170534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453536-A-T

http://identifiers.org/hco/8/GRCh38#43170548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26453522-A-C

43170566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453503-T-C

43170573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453496-T-A

43170573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453496-T-C

43170639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26453430-A-G

43170737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453355-A-G

43170737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453355-A-T

43170780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26453310-A-G

43171420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26452166-G-A

43171897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451843-A-G

43171909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451831-G-T

43172012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451740-T-A

43172014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451738-T-C

43172060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451692-A-G

43172060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26451692-A-T

http://identifiers.org/hco/8/GRCh38#43172246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26450971-C-A

43172246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450971-C-G

43172257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450960-T-C

43172397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450841-T-C

http://identifiers.org/hco/8/GRCh38#43172460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26450793-C-A

43172460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450793-C-G

43172460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450793-C-T

43172570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450713-G-T

43172728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450577-A-G

43172777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450528-G-C

43172826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26450480-T-C

43172939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26449788-G-A

http://identifiers.org/hco/8/GRCh38#43173652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26449706-A-C

43173652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26449706-A-G

43173679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26449678-G-A

43173679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26449678-G-T

43173721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26449631-G-A

43173913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 26448836-G-T

43177831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447608-C-T

43177857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447582-C-G

43177920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447523-C-T

http://identifiers.org/hco/8/GRCh38#43177952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26447491-A-C

43177982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447460-T-A

43177997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447450-G-T

http://identifiers.org/hco/8/GRCh38#43177998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26447449-C-A

43178004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447443-A-T

43178034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447414-T-A

http://identifiers.org/hco/8/GRCh38#43178045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26447403-C-A

43178045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447403-C-T

43178175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, missense_variant
orthologous variants: 26447275-G-A

43178228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, missense_variant
orthologous variants: 26447222-G-A

43178228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, missense_variant
orthologous variants: 26447222-G-T

43178283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447165-A-G

43178285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447163-T-C

43178288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447158-A-G

http://identifiers.org/hco/8/GRCh38#43178310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26447011-C-A

43178310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26447011-C-T

43178322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26446999-C-T

43178357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26446965-G-A

43178357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26446965-G-T

43178363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron variant
orthologous variants: 26446959-A-G

43181726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446126-T-G

43181732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446120-G-A

43181732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446120-G-T

43181734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446118-A-G

43181759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446091-G-A

43181774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26446076-A-G

43181892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445974-G-A

http://identifiers.org/hco/8/GRCh38#43181985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26445950-C-A

43181985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445950-C-T

http://identifiers.org/hco/8/GRCh38#43181986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26445949-A-C

43181986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445949-A-G

http://identifiers.org/hco/8/GRCh38#43182075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26445880-C-A

http://identifiers.org/hco/8/GRCh38#43182081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26445878-A-C

43182081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445878-A-G

43182100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445859-G-A

43182101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445858-G-A

43182101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445858-G-T

43182110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26445849-T-C

43182207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26445753-G-A

http://identifiers.org/hco/8/GRCh38#43182234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26445726-A-C

43182234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26445726-A-T

43192254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443487-G-C

43192254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443487-G-T

43192335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26443402-T-A

43192450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443287-G-A

43192478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443273-A-G

43192905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443042-G-A

43192947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442999-G-A

43192965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442981-C-T

43193057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442923-G-C

43193073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442907-C-G

43193165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442749-C-G

43193605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442309-G-T

43193701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442140-T-G

http://identifiers.org/hco/8/GRCh38#43193706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26442135-C-A

43193706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442135-C-T

43193888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26441932-T-C

43193897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26441918-C-T

43193947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26441868-T-C

43193953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26441862-A-G

43194043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26441778-T-C

43196675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438279-G-A

43196675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438279-G-T

43196717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438248-T-C

http://identifiers.org/hco/8/GRCh38#43196734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26438231-C-A

43196821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438160-A-T

43196836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438145-T-C

43196869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438111-T-C

43196874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438106-A-T

43196889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438093-T-C

http://identifiers.org/hco/8/GRCh38#43196906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26438077-C-A

43196906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438077-C-G

43196906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26438077-C-T

43197046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437939-G-A

43197046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437939-G-C

43197046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437939-G-T

http://identifiers.org/hco/8/GRCh38#43197189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26437348-A-C

43197189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437348-A-G

http://identifiers.org/hco/8/GRCh38#43197219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26437318-C-A

43197254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437273-C-T

43197290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437240-T-A

43197290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437240-T-C

43197290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437240-T-G

43197291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437239-G-T

43197298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437232-G-A

43197298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26437232-G-C

43197428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26436766-G-T

43197490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26436710-G-T

43197554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26436650-A-T

http://identifiers.org/hco/8/GRCh38#43197566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26436636-C-A

43197643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26436569-T-C

43197859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26436355-A-G

43197900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26436314-C-G

43197900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26436314-C-T

43197904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26436310-G-C

43197932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26436282-G-A

43197932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26436282-G-T

43197974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436249-A-G

43197988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436236-G-A

43197989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436235-T-C

43197991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436233-A-T

43198001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436223-A-G

43198017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436209-G-A

43198017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436209-G-T

43198033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436193-T-C

43198037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436189-G-A

43198037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436189-G-T

43198066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436169-T-C

http://identifiers.org/hco/8/GRCh38#43198113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26436123-A-C

43198151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436087-C-T

43198165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436072-C-T

43199311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26435394-G-A

43199311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26435394-G-T

43199334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26435371-T-G

http://identifiers.org/hco/8/GRCh38#43199356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#26435367-A-C

43199356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26435367-A-G

43199531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26435198-T-C

43199532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26435197-A-G

43199621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435108-G-A

43199621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435108-G-T

43199637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435092-G-A

43199637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435092-G-C

43199637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435092-G-T

43199690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435064-G-A

43199690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26435064-G-T

http://identifiers.org/hco/8/GRCh38#43199956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26434739-C-A

43199956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434739-C-T

http://identifiers.org/hco/8/GRCh38#43199977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26434719-A-C

43199977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434719-A-G

43199982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434714-A-G

43199998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434698-T-C

http://identifiers.org/hco/8/GRCh38#43200257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26434427-C-A

43200299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434364-G-T

43200350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434332-T-C

43200466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434214-C-T

43200482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434198-G-A

43200482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26434198-G-T

http://identifiers.org/hco/8/GRCh38#43201207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432945-C-A

43201207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432945-C-G

43201207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432945-C-T

43201261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432886-T-C

43201397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432814-T-C

http://identifiers.org/hco/8/GRCh38#43201404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432807-C-A

43201404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432807-C-T

http://identifiers.org/hco/8/GRCh38#43201415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432794-C-A

43201417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432792-G-A

43201417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432792-G-T

http://identifiers.org/hco/8/GRCh38#43201511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432761-A-C

43201511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432761-A-G

43201511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432761-A-T

http://identifiers.org/hco/8/GRCh38#43201663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432622-C-A

http://identifiers.org/hco/8/GRCh38#43201679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432606-C-A

43201679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432606-C-T

http://identifiers.org/hco/8/GRCh38#43201774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26432547-C-A

43201826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432494-A-G

43201876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432445-G-A

43201878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26527
most severe consequence: 3 prime UTR variant
orthologous variants: 26432443-A-T