42013641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126590-C-T

42013719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 121126679-C-T

42013850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126742-G-A

42013850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126742-G-T

42013880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126756-G-T

42014031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126830-G-A

42014031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126830-G-C

42014031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121126830-G-T

42014178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121126938-A-G

42014337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121127026-G-T

42014346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127036-A-T

42014358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127048-G-C

42014416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127106-C-T

42014541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127212-T-C

42014711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127350-G-C

42015018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121127646-G-T

http://identifiers.org/hco/3/GRCh38#42015346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121127992-A-C

42015410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128067-G-A

42015662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128334-T-A

42015719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128396-T-A

42015719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128396-T-C

42016729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128724-G-A

42016806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121128753-G-A

42017473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121129156-G-A

42017473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121129156-G-T

42019387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121131907-C-G

42019387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121131907-C-T

42019427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121131937-G-C

42019449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121131959-A-T

42019877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121132323-A-G

42020920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121134867-G-A

42020920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121134867-G-C

42021013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121134952-C-G

42021195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121135138-T-G

42021333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121135204-A-G

42021335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121135206-G-T

42021498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121135480-G-T

42022072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121136372-A-G

42022412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121136736-G-A

42023014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121138035-T-C

42023026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121138048-T-C

http://identifiers.org/hco/3/GRCh38#42023157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121138167-C-A

http://identifiers.org/hco/3/GRCh38#42023264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121138243-A-C

42023265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121138244-A-G

42024621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141501-G-A

42024970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141778-T-A

42025089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141873-C-T

http://identifiers.org/hco/3/GRCh38#42025154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121141931-C-A

42025154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141931-C-G

42025154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141931-C-T

42025197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121141975-T-G

42025436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143043-A-G

42025654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143217-G-T

42025678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143241-T-G

42025827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143377-G-C

42025872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143422-T-G

42025940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143492-A-G

42026034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143577-G-A

42026034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143577-G-C

42026034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143577-G-T

http://identifiers.org/hco/3/GRCh38#42026100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121143640-C-A

42026100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121143640-C-T

42028377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121144844-A-T

42028547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121144930-T-A

42028668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121145048-G-T

42030905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121145583-A-G

42030905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121145583-A-T

42031863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121146694-G-A

http://identifiers.org/hco/3/GRCh38#42031939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121146759-C-A

42032003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121146848-T-A

http://identifiers.org/hco/3/GRCh38#42033187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121148758-C-A

42033361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121148930-G-A

42037336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121158575-T-G

42037415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121158625-C-T

42037431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121158640-A-G

42037441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121158650-C-T

42051259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121164745-C-T

42051320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121164786-G-A

42051320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121164786-G-T

42051427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121164871-A-G

http://identifiers.org/hco/3/GRCh38#42051469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121164883-C-A

42051546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121164960-T-C

42051557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121164971-T-A

http://identifiers.org/hco/3/GRCh38#42051559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121164973-C-A

http://identifiers.org/hco/3/GRCh38#42051562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121164976-C-A

42051780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121165029-T-C

http://identifiers.org/hco/3/GRCh38#42051829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121165060-C-A

42052027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121165229-T-G

42052051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121165252-A-G

42054834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121168559-A-G

42057099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171161-A-G

42057209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171263-A-G

42057298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171312-A-T

42057306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171319-C-T

42057325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171338-C-T

42057907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121171889-A-G

42058085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121172059-T-C

42059515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121172967-C-T

42059777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121173183-T-G

42060052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121173547-T-A

42060131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121173612-G-A

42060887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174176-G-A

42060891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174180-A-G

42060926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174214-C-T

42060973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174288-A-T

42061032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174341-T-G

42061158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121174469-C-T

http://identifiers.org/hco/3/GRCh38#42061363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121174569-A-C

http://identifiers.org/hco/3/GRCh38#42061710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121174905-C-A

42061808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121175666-A-T

42062174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176005-A-G

42062235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176062-A-T

42062239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176066-T-G

42062547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176291-G-C

42062684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176387-G-T

42062726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176432-A-G

42062748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176451-A-G

42063012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121176842-A-G

42064457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121177185-T-A

42064536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121177260-A-T

42064556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121177280-A-G

42066731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121180032-G-A

42067293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121180523-A-G

42067376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121180605-G-T

42067595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121180823-T-C

42067737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121180935-G-A

42071788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121184399-C-G

42071843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121184454-A-G

42071980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121184603-T-C

42072017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121184632-T-C

42072017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121184632-T-G

42072259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121184857-G-T

42072359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121184954-T-C

42072766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121185311-G-C

42072803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121185348-T-C

42073065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186369-C-T

42073071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186375-C-T

42073087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186391-C-T

42073098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186402-C-T

42073213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186520-T-C

42073386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121186817-G-A

42073650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187131-T-C

42073695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187160-A-G

42073791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187236-G-A

42073820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187265-G-T

42074267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187620-C-T

42074294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121187632-A-T

42074508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121188667-T-G

42074509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121188668-G-A

42080605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, undefined
orthologous variants: 121189754-A-G

42087056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121193016-T-G

http://identifiers.org/hco/3/GRCh38#42087074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121193037-C-A

42087078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron variant
orthologous variants: 121193041-G-A

42087099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121193062-C-T

42087125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5 prime UTR variant
orthologous variants: 121193088-C-T

42087154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5 prime UTR variant
orthologous variants: 121193118-T-C

42087345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121193310-G-A

42087345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121193310-G-T

42087440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121193401-G-A

42087440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121193401-G-T

42087560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121193828-A-G

42087767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121193979-A-G

42090804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195546-G-C

42090937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195666-G-A

42090937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195666-G-T

http://identifiers.org/hco/3/GRCh38#42090938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121195667-C-A

42090938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195667-C-T

42090944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195673-T-C

42090944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195673-T-G

42090968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195697-A-G

42090978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195707-C-T

42091134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195846-C-T

42091230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195948-G-A

42091230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195948-G-C

42091230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121195948-G-T

http://identifiers.org/hco/3/GRCh38#42091285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121196005-C-A

42091285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196005-C-T

http://identifiers.org/hco/3/GRCh38#42091628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121196340-C-A

42091628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196340-C-T

42091704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196410-A-G

42091704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196410-A-T

42091793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196678-C-G

42091793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196678-C-T

42091826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196714-C-T

42092023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196911-G-A

42092066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121196952-C-T

42092524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121197337-A-G

42092557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121197368-A-G

42093048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121198004-T-A

42093088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121198042-A-G

42093168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121198114-A-G

42098087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121201668-C-G

42098120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121201700-T-G

42098124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121201704-C-T

42099092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202714-G-A

42099130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202756-G-C

42099130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202756-G-T

42099267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202872-G-T

42099284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202893-G-A

42099284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121202893-G-C

42099529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121203102-G-A

42107595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121204295-A-G

42107610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121204310-A-T

42107732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121204385-C-T

42107894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121204549-G-C

http://identifiers.org/hco/3/GRCh38#42108530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121205211-C-A

42108833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121205522-C-T

42108838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121205527-T-A

42109459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121206280-G-A

42109459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121206280-G-C

42115412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121211932-C-T

42116162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121212509-C-T

42116164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121212511-C-G

42116164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121212511-C-T

http://identifiers.org/hco/3/GRCh38#42116290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121212612-A-C

42116291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121212613-G-A

42116291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121212613-G-C

http://identifiers.org/hco/3/GRCh38#42116431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121212845-A-C

42116689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213068-G-T

42116783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213137-G-A

42116880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213225-C-T

42116914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213262-A-G

42116979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213327-T-C

42116995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121213349-C-G

42117382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214386-G-A

42117382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214386-G-C

42117382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214386-G-T

42117384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214388-G-A

42117384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214388-G-T

42117425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214430-C-G

42117453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121214444-C-T

42117649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121214590-C-T

42117663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121214603-C-T

42117664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121214604-G-A

42122038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216646-G-A

42122038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216646-G-T

http://identifiers.org/hco/3/GRCh38#42122064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121216663-A-C

42122086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216684-G-A

42122097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216695-T-C

42122109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216707-C-T

42122116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121216718-G-A

http://identifiers.org/hco/3/GRCh38#42122272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121216991-A-C

42122574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217300-C-T

42122769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217453-T-C

42122789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217471-G-A

42122789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217471-G-C

42122983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217714-T-A

42122983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217714-T-G

42123031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217762-C-G

42123044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217775-G-A

42123048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217779-T-A

42123092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121217818-C-T

42124629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219086-G-A

42124656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219113-C-T

42124819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219265-A-G

42124872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219321-C-T

http://identifiers.org/hco/3/GRCh38#42124944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121219429-A-C

42124951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219436-G-A

42124951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219436-G-T

42124983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219475-A-G

42125034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121219523-A-G

42125283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121220799-C-T

42125328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121220847-G-A

42125328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121220847-G-T

42125357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121220869-G-A

42125430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121220933-C-T

42125600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121221103-C-T

42125717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221179-T-A

42125731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221193-A-G

42125731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221193-A-T

42125755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221218-A-T

http://identifiers.org/hco/3/GRCh38#42125764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121221227-C-A

42125764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221227-C-G

42125764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221227-C-T

42125766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221229-G-A

42125766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121221229-G-T

http://identifiers.org/hco/3/GRCh38#42126907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121222996-A-C

42126945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223025-G-A

42127047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223076-A-G

http://identifiers.org/hco/3/GRCh38#42127099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121223129-A-C

http://identifiers.org/hco/3/GRCh38#42127195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121223206-A-C

42127232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223233-T-G

42127235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223236-T-C

42127705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223364-A-T

42127719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223377-G-A

42128211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223487-A-T

42128385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223629-C-G

42128539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121223969-C-G

42129193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121225038-C-T

42129205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121225050-T-G

42129339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121225197-C-T

42139513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227419-T-C

http://identifiers.org/hco/3/GRCh38#42139563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121227442-A-C

42139972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227820-C-T

42140015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227864-C-T

42140016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227865-C-T

42140101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227938-G-C

42140130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121227967-G-T

42140320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121228101-G-C

42142326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121229517-T-G

http://identifiers.org/hco/3/GRCh38#42142609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121229791-A-C

42142658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121229839-T-C

http://identifiers.org/hco/3/GRCh38#42148278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121231564-A-C

42148510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121231828-A-G

42148687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121231976-A-G

42148923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121232202-C-G

42149139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121232406-G-A

42149160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121232427-T-C

42149160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121232427-T-G

http://identifiers.org/hco/3/GRCh38#42149259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121232525-C-A

42149259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232525-C-G

42149259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232525-C-T

http://identifiers.org/hco/3/GRCh38#42149333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121232603-C-A

42149333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232603-C-T

42149370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232640-T-C

42149393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232663-G-A

42149393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232663-G-T

http://identifiers.org/hco/3/GRCh38#42149618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121232889-A-C

42149637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232905-A-G

42149680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232947-T-C

42149684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232951-G-A

42149707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121232979-G-T

http://identifiers.org/hco/3/GRCh38#42149744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121233011-C-A

42149800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233067-C-T

http://identifiers.org/hco/3/GRCh38#42149873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121233149-C-A

42149999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233237-G-C

42150106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233337-G-A

42150164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233395-T-G

42150254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233485-A-G

http://identifiers.org/hco/3/GRCh38#42150260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121233491-A-C

42150345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233574-G-A

42150494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233713-T-C

42150498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233717-G-A

42150672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233886-A-G

42150680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121233894-C-G

42150810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234013-C-T

42150885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234080-G-A

42150923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234117-C-G

42151190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234312-T-C

http://identifiers.org/hco/3/GRCh38#42151370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121234463-C-A

42151370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121234463-C-G

42151381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121234474-T-C

42151398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121234489-G-A

42151422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234512-A-G

42151448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234532-T-C

http://identifiers.org/hco/3/GRCh38#42151483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121234566-A-C

42151483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234566-A-G

42151696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121234722-C-G

42151989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121235116-G-A

42151993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121235119-G-A

42152133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121235281-C-G

42158365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121243567-C-T

42159155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244090-G-A

42159197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244131-T-C

42159697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244587-G-A

http://identifiers.org/hco/3/GRCh38#42160020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121244894-C-A

42160020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244894-C-T

http://identifiers.org/hco/3/GRCh38#42160027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121244901-C-A

42160041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121244917-G-A

http://identifiers.org/hco/3/GRCh38#42160070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121244946-C-A

42160070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244946-C-G

42160070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121244946-C-T

http://identifiers.org/hco/3/GRCh38#42160203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121245076-C-A

42160203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121245076-C-T

http://identifiers.org/hco/3/GRCh38#42160244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121245117-A-C

42160244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121245117-A-G

http://identifiers.org/hco/3/GRCh38#42160278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121245145-C-A

42160298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121245165-G-A

42160439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121245306-C-G

42160439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 121245306-C-T

http://identifiers.org/hco/3/GRCh38#42160461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121245328-C-A

42160533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245452-A-G

42160533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245452-A-T

42160551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245472-T-A

42160551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245472-T-C

42160551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245472-T-G

42160564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245473-T-A

42160564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245473-T-G

42160622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245514-G-A

42160622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245514-G-C

42160622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245514-G-T

42160669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245554-C-T

42160786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245670-A-G

42160896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245773-C-T

42160920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245796-G-C

42160920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121245796-G-T

42161156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246130-A-G

42161230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246198-C-T

42161300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246272-C-G

42161300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246272-C-T

42161751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246447-G-T

42162262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121246870-G-A

42166114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121251389-C-G

42166207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121251485-A-G

42166299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121251547-G-A

42166392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121251639-G-C

42166869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121252362-C-T

42168324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121252851-T-C

42168376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121252900-G-A

42168381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121252905-G-A

42168433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121252981-G-A

42168465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253012-G-A

42169203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253129-A-G

42169227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253156-G-T

42169235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253164-G-A

42169235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253164-G-C

42169305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253235-A-G

42169505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253426-A-G

42169654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253464-A-G

42169760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253512-G-A

42169909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253627-G-A

42170200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253909-G-A

42170267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121253973-T-C

42170849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254523-A-G

42170902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254577-C-G

42171058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254674-G-A

42171081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254697-C-T

42171106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254704-C-T

42171180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254773-G-A

42171467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121254996-A-G

42171528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255056-A-G

http://identifiers.org/hco/3/GRCh38#42172028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121255417-A-C

42172047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255432-G-A

42172126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255476-G-A

42172155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255508-T-C

42172158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255511-A-G

42172309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255649-A-G

42172309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255649-A-T

42172506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121255819-C-T

42175307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121259411-C-T

42175778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121259879-G-A

42175778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121259879-G-T

42175792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121259893-T-G

42176187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260164-G-C

42176189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260166-G-A

42176215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260196-C-G

42176660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260423-G-A

42176708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260461-T-C

42176709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260462-G-A

42176712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260465-T-C

42176741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260488-C-T

42176770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260501-G-A

42176778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260509-C-T

42176792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260523-T-C

42176848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121260579-G-A

42176848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121260579-G-C

42177015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121260717-T-C

42177344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121261536-A-G

42177465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121261658-G-A

42177741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121262514-G-T

42177791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121262564-C-T

42177805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121262578-C-T

http://identifiers.org/hco/3/GRCh38#42177807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121262580-A-C

http://identifiers.org/hco/3/GRCh38#42179418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121264646-C-A

42179418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121264646-C-T

42180884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121265577-A-G

42181021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121265718-G-A

42181611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121266207-A-T

42181621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121266218-G-C

42183731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121267769-A-T

42183771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121267808-A-G

42183986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121267993-T-C

42184078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121268084-C-T

http://identifiers.org/hco/3/GRCh38#42184555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121269618-A-C

42184555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121269618-A-G

42184577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121269640-T-C

42184577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121269640-T-G

42184589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121269652-G-T

42184619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121269673-G-A

42184692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121269743-G-A

42184692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121269743-G-T

42184889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121269897-T-C

42184889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121269897-T-G

http://identifiers.org/hco/3/GRCh38#42184918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121269930-C-A

42184918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121269930-C-G

42184918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121269930-C-T

42185049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270018-G-T

42185128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270063-A-T

42185286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270120-G-A

42185325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270153-A-T

42185431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270231-G-C

42185515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270311-A-G

42185547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270343-C-T

42186461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270600-T-A

42186474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270617-G-C

42186663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121270766-C-T

42186938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271035-T-G

42187001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271083-T-C

42187069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271152-C-T

42187206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271279-C-T

42187217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271290-T-A

42187307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271364-A-G

42187314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271371-G-T

42187388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271444-T-C

42187893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271645-T-C

http://identifiers.org/hco/3/GRCh38#42187947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121271669-A-C

42188080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121271793-T-G

42188092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121271805-G-A

42188125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121271838-C-G

42188125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121271838-C-T

http://identifiers.org/hco/3/GRCh38#42188239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121271949-A-C

http://identifiers.org/hco/3/GRCh38#42188276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121271974-C-A

42188276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271974-C-T

42188291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121271987-G-A

42188409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272100-A-G

42188454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272143-C-T

42188479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272156-T-G

42188664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272298-G-C

http://identifiers.org/hco/3/GRCh38#42188922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121272604-C-A

42188922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272604-C-T

42188941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272625-T-C

42188971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272649-G-A

42188981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272659-G-A

42188981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272659-G-C

42189000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272677-G-A

42189165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272838-G-A

42189191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272853-G-A

42189191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272853-G-C

42189191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272853-G-T

http://identifiers.org/hco/3/GRCh38#42189194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121272856-C-A

42189194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272856-C-T

http://identifiers.org/hco/3/GRCh38#42189929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121273186-C-A

42190563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273787-C-G

42191328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274641-G-A

42191399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274712-A-G

42191414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274727-T-C

42191414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274727-T-G

42191415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274728-T-G

42191436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274748-G-A

42191464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274777-G-A

42191464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274777-G-T

http://identifiers.org/hco/3/GRCh38#42191476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121274789-C-A

http://identifiers.org/hco/3/GRCh38#42191511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121274823-C-A

42191511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274823-C-G

42191511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274823-C-T

http://identifiers.org/hco/3/GRCh38#42191515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121274827-C-A

42191515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274827-C-T

http://identifiers.org/hco/3/GRCh38#42191567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121274890-C-A

42191567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121274890-C-T

42191602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121274925-G-A

http://identifiers.org/hco/3/GRCh38#42191650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121274980-C-A

42191650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274980-C-T

42191654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274984-T-C

42191659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274989-T-C

42191743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275036-A-G

42191853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275126-G-A

42192962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275679-T-C

42193085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 121275766-T-C

http://identifiers.org/hco/3/GRCh38#42193160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121275841-A-C

42193160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121275841-A-G

42193294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275960-G-T

42193295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275961-T-C

42193367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276029-A-G

42193382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276042-G-A

42193448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276114-T-C

http://identifiers.org/hco/3/GRCh38#42193563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121276265-A-C

42193566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276268-T-C

42193715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277070-A-G

http://identifiers.org/hco/3/GRCh38#42193746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121277101-A-C

42193806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277157-A-G

42193929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277279-C-T

http://identifiers.org/hco/3/GRCh38#42193955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121277298-C-A

42193955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277298-C-T

42193956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277299-C-G

42193956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277299-C-T

42193971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277314-T-A

42193989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277332-C-T

42193994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277337-G-T

42194058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277378-C-T

42194603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277736-G-A

42194670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277783-G-T

http://identifiers.org/hco/3/GRCh38#42194675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121277788-C-A

42194675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277788-C-T

42194682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277795-G-A

42194682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277795-G-C

42194682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277795-G-T

42194720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277804-G-A

42194720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277804-G-T

http://identifiers.org/hco/3/GRCh38#42194730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121277814-C-A

42194730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277814-C-T

42194732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277816-T-G

42194740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277824-G-C

42194751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277835-G-A

42194751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277835-G-C

42194751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277835-G-T

42194827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277911-C-T

42194830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277914-A-G

42194867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277951-C-T

http://identifiers.org/hco/3/GRCh38#42194890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121277974-C-A

42194890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277974-C-T

42194905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277983-G-A

42194905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121277983-G-C

42195038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278119-G-T

42195157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121278204-C-G

42198846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280393-A-G

42198850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280397-G-A

http://identifiers.org/hco/3/GRCh38#42199059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121280603-C-A

42199070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280614-T-C

http://identifiers.org/hco/3/GRCh38#42199096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121280637-C-A

42199096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280637-C-G

42199096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280637-C-T

42199106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280647-G-A

42199106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280647-G-T

42199112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280653-C-T

42199258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280798-G-A

42199258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280798-G-C

42199261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121280803-C-T

42199310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280846-A-G

42199310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280846-A-T

http://identifiers.org/hco/3/GRCh38#42199322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121280858-C-A

42199325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280861-G-T

42199328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280863-A-G

42199398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280928-A-G

42199905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281361-G-A

42200003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281497-G-A

42200046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281528-T-C

42200085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281573-A-G

42200177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281732-T-C

42200216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281768-C-T

42200353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281901-C-T

42200375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281927-A-G

42200451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281962-G-A

42200452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281963-C-T

42200507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282014-A-T

42200513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282020-G-T

42200555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282061-A-G

42200562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282068-T-C

42200661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282156-T-C

42200683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282177-G-A

42200683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282177-G-T

42200695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282189-A-G

42200713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282199-T-C

42200852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121282308-A-G

42200869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121282325-G-T

42200884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121282340-C-T

42201081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282531-T-C

42201102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282549-G-A

42201156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282564-T-A

42201156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282564-T-C

42201156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282564-T-G

42201193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282581-T-A

42201193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282581-T-C

42201193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282581-T-G

42201497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282619-G-C

42201826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282865-C-G

http://identifiers.org/hco/3/GRCh38#42201930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121282906-A-C

42201948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282920-C-T

42201970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282942-A-G

42201984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121282955-C-T

42202096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283062-A-G

42202247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283210-C-T

42202250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283213-C-G

42202250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283213-C-T

http://identifiers.org/hco/3/GRCh38#42202294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283236-C-A

http://identifiers.org/hco/3/GRCh38#42202312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283243-C-A

42202317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283248-G-A

42202317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283248-G-T

http://identifiers.org/hco/3/GRCh38#42202404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283317-C-A

42202404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283317-C-T

42202422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283333-C-G

42202422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121283333-C-T

http://identifiers.org/hco/3/GRCh38#42202439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283348-C-A

42202439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121283348-C-T

42202460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121283369-G-A

42202460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121283369-G-C

42202460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121283369-G-T

42202556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121283465-T-A

42202919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283828-G-T

http://identifiers.org/hco/3/GRCh38#42202937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283841-C-A

42203000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283881-T-A

42203000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283881-T-G

42203024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283894-C-T

http://identifiers.org/hco/3/GRCh38#42203072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121283937-C-A

42203074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283939-C-T

42203114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283997-G-A

42203114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121283997-G-T

http://identifiers.org/hco/3/GRCh38#42203122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121284005-A-C

42203122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284005-A-G

42203180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284055-A-T

42203190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284065-A-G

42203232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284105-A-G

42203276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284155-T-C

42203294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284173-G-A

42203294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284173-G-T

42203316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284207-C-G

42203316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284207-C-T

42203331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284222-T-C

42203364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284255-G-A

42203368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284259-G-A

42203413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284302-G-A

42203413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284302-G-T

42203452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284306-A-G

42203452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284306-A-T

42203464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284318-C-G

42203464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284318-C-T

http://identifiers.org/hco/3/GRCh38#42203468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121284322-C-A

42203468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284322-C-G

42203468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284322-C-T

42203620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284425-A-G

42203650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284455-T-C

42203689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284488-G-A

42203721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284516-T-C

42203728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284523-C-T

42203778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284580-A-G

42204008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284749-A-G

42204057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121284813-G-A

42204215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121284972-T-C

42204289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285034-A-G

42204325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285070-T-G

http://identifiers.org/hco/3/GRCh38#42204837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121285312-C-A

42205014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285426-C-T

http://identifiers.org/hco/3/GRCh38#42205040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121285458-C-A

42205084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285492-A-G

http://identifiers.org/hco/3/GRCh38#42205203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121285545-A-C

42205203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285545-A-G

42205302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285628-G-T

42205354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285681-A-G

42205470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285801-T-C

42205534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121285851-A-G

42206216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121286142-C-T

42207269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121286634-G-T

42207273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121286638-T-C

http://identifiers.org/hco/3/GRCh38#42207300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121286663-A-C

42208237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121287957-G-A

42208604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288245-A-G

42208826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288433-A-G

http://identifiers.org/hco/3/GRCh38#42208976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121288554-A-C

42209098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288673-C-T

42209350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288826-T-C

42209353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288829-G-T

42209385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288853-T-C

http://identifiers.org/hco/3/GRCh38#42209624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289154-C-A

42209624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289154-C-T

42209659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289291-G-A

42209659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289291-G-T

http://identifiers.org/hco/3/GRCh38#42209739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289405-C-A

42209739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289405-C-T

42209828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121289486-C-T

http://identifiers.org/hco/3/GRCh38#42210077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289735-A-C

42210132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121289790-A-G

http://identifiers.org/hco/3/GRCh38#42210185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289843-C-A

http://identifiers.org/hco/3/GRCh38#42210192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289850-A-C

http://identifiers.org/hco/3/GRCh38#42210265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289924-A-C

42210316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121289973-A-G

http://identifiers.org/hco/3/GRCh38#42210336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121289990-C-A

42210337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121289991-T-C

42210384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290028-T-C

42210384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290028-T-G

42210427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290054-T-A

42210427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290054-T-C

42210427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290054-T-G

42210457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290083-C-T

http://identifiers.org/hco/3/GRCh38#42210459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121290085-C-A

42210459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290085-C-G

42210473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290100-G-T

42210534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290164-T-C

http://identifiers.org/hco/3/GRCh38#42210587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121290201-A-C

42210587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290201-A-G

42210587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290201-A-T

http://identifiers.org/hco/3/GRCh38#42210594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121290208-A-C

42210594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290208-A-G

42210627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290241-G-A

42210627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290241-G-C

42210627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290241-G-T

42210647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290261-T-C

42210647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290261-T-G

42210663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290277-T-C

42210663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290277-T-G

http://identifiers.org/hco/3/GRCh38#42210989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121290569-C-A

42211010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290588-G-A

42211010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290588-G-T

42211020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290598-T-C

42211145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290697-G-A

42211183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290729-C-T

42211218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290763-G-T

42211231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290779-A-G

42211406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290915-T-C

42211415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121290924-G-T

42211983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291128-G-A

42212009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291156-C-T

42212053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291222-G-C

42212105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291261-A-G

42212116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291272-C-G

42212116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291272-C-T

42212154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291315-T-C

42212195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291360-T-C

http://identifiers.org/hco/3/GRCh38#42212237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121291399-A-C

42212237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291399-A-G

42212248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291407-G-A

42212257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291416-T-C

42212317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291428-A-G

42212360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291470-A-G

42212401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121291504-A-G

42213353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292059-G-A

42213617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292314-C-G

42213617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292314-C-T

42213635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292323-G-A

42213706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292392-G-C

42213906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292593-G-A

42214127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121292814-T-C

42214422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293130-A-G

42214454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293162-A-G

42214480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293188-T-C

42214480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293188-T-G

42214492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293200-T-C

42214735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293486-A-G

42214783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293536-G-C

42214786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293538-C-T

42215156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121293956-T-A

42215323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294075-C-G

42215323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294075-C-T

http://identifiers.org/hco/3/GRCh38#42215348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121294094-A-C

42215348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294094-A-T

42215606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294371-G-A

42215931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294784-G-T

42216067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121294900-G-A

42216260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295069-T-C

42216775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295433-A-T

http://identifiers.org/hco/3/GRCh38#42216896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121295692-A-C

42216906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295702-A-G

42216924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295720-C-G

42216929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295726-T-C

42217002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295783-G-A

42217073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295843-T-C

http://identifiers.org/hco/3/GRCh38#42217079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121295849-A-C

42217079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121295849-A-T

42217191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121295921-C-G

42217191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121295921-C-T

42217270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121296000-G-T

42217353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296083-T-G

42217365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296092-G-C

42217389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296114-A-G

42217392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296117-C-T

42217488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296214-A-G

42217505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296231-T-C

42217544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296259-G-T

42217935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296606-A-G

42217948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296617-T-A

42217952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296621-T-G

42217963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296632-C-T

42218201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296890-A-G

42218201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296890-A-T

42218218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296907-C-T

42218319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296967-A-G

42218320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296968-G-C

42218320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296968-G-T

42218339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121296983-C-T

42218379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121297018-T-C

42218417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121297050-G-C

42218525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121297147-A-T

42218806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297413-G-A

42218806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297413-G-T

42219102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297666-C-G

42219102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297666-C-T

42219273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121297826-G-A

42219435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121297986-T-A

http://identifiers.org/hco/3/GRCh38#42220176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121298923-C-A

42220195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298942-C-T

42220360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299104-T-C

42220360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299104-T-G

42220404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299170-C-G

42220628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299423-C-T

42220863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299651-G-A

42220863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299651-G-T

42220911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299696-T-G

42220920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299706-T-A

42220920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299706-T-C

42220926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299712-C-T

http://identifiers.org/hco/3/GRCh38#42220930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121299716-C-A

42220930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299716-C-T

42221068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299881-G-A

42221115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299911-C-G

42221125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299926-T-A

42221175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299955-C-G

42221175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299955-C-T

42221413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300174-G-A

42222088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300554-A-G

42222334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300795-C-T

http://identifiers.org/hco/3/GRCh38#42222422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121300829-A-C

42222691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301081-G-A

http://identifiers.org/hco/3/GRCh38#42222804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121301181-C-A

42222804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301181-C-T

http://identifiers.org/hco/3/GRCh38#42222828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121301205-C-A

42222828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301205-C-G

42222915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301272-T-G

42222916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301273-G-A

42222916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301273-G-T

http://identifiers.org/hco/3/GRCh38#42222922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121301279-C-A

42222922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301279-C-G

42222922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121301279-C-T

42222963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121301324-A-G

42222975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121301336-C-G

42222975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121301336-C-T

http://identifiers.org/hco/3/GRCh38#42222976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121301337-A-C

42222976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121301337-A-G

42223374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121301738-G-A

http://identifiers.org/hco/3/GRCh38#42223999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121302290-A-C

42224008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302299-T-A

42224050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302341-T-A

http://identifiers.org/hco/3/GRCh38#42224141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121302441-A-C

42224233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302481-T-A

http://identifiers.org/hco/3/GRCh38#42224257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121302499-C-A

42224257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302499-C-G

42224257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302499-C-T

42224281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302527-G-C

42224281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302527-G-T

42224362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302596-C-T

http://identifiers.org/hco/3/GRCh38#42224463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121302695-C-A

42224771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121302991-G-A

42224836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303044-G-A

42224836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303044-G-T

42224908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303108-A-G

42225039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303232-G-C

42225152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303379-T-C

http://identifiers.org/hco/3/GRCh38#42225155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121303382-C-A

42225155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303382-C-T

42225217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303442-G-A

42225370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303598-A-G

42225387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303615-G-T

http://identifiers.org/hco/3/GRCh38#42225451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121303676-C-A

http://identifiers.org/hco/3/GRCh38#42225561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121303775-C-A

42225621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29947
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121303837-G-T