90000990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, undefined
orthologous variants: 79675604-A-G

90001669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79676269-G-T

90001688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79676287-G-A

http://identifiers.org/hco/15/GRCh38#90001728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79676328-A-C

90001838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79676424-G-A

90001976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79676677-A-T

90002235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79676935-G-A

90002599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79677230-A-G

90002599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79677230-A-T

90002619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79677250-G-A

90003087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79677590-G-T

90003514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79677907-T-C

90003591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79677974-G-T

90003880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678233-T-C

90004005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678333-G-A

90004082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678413-G-A

90004193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678508-T-C

90004257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678572-G-T

90004315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79678744-T-G

http://identifiers.org/hco/15/GRCh38#90004387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79678997-A-C

90004409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679018-T-C

90004439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679049-T-A

http://identifiers.org/hco/15/GRCh38#90004671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79679227-A-C

90004671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679227-A-T

http://identifiers.org/hco/15/GRCh38#90004792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79679354-C-A

90004792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679354-C-T

90004806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679370-G-A

90004806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679370-G-T

90004965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679520-A-G

90005021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679574-A-T

90005027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679581-A-G

90005072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679626-A-G

http://identifiers.org/hco/15/GRCh38#90005086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79679640-A-C

90005286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79679900-G-A

90005366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, undefined
orthologous variants: 79679980-G-T

90006299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79681041-A-G

90006864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79682357-C-G

90007216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79682698-G-T

90007308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79682786-C-T

90007946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684274-C-G

90008241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684551-C-T

90008822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684730-A-G

90008856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684762-G-A

90008856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684762-G-T

90008974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684872-C-T

90008997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79684892-A-G

90009158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685036-G-A

90009178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685055-G-A

90009510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685336-C-T

90009644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685446-C-G

90010087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685682-C-G

90010087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79685682-C-T

90010392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, undefined
orthologous variants: 79686065-G-A

90010480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79686133-G-C

90010492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79686145-T-C

90016693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690280-T-C

90016752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690334-C-G

90016820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690380-C-G

90016923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690482-G-T

90016952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690511-G-C

90017244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79690864-T-C

90017293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691051-T-C

90017349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691107-T-C

90017431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691190-G-A

90017431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691190-G-C

90017431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691190-G-T

90017444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691197-C-T

90017818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691472-G-C

90017999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691646-C-T

http://identifiers.org/hco/15/GRCh38#90018140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79691786-C-A

http://identifiers.org/hco/15/GRCh38#90018189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79691829-A-C

90018189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691829-A-G

90018189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691829-A-T

http://identifiers.org/hco/15/GRCh38#90018190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79691830-A-C

90018190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691830-A-T

http://identifiers.org/hco/15/GRCh38#90018197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79691837-C-A

90018197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691837-C-T

http://identifiers.org/hco/15/GRCh38#90018215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79691852-C-A

90018234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691875-T-C

90018249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691890-A-T

90018318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691945-G-A

90018397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79691993-A-G

90018460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79692016-G-A

90018600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79692114-C-T

90019150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79692696-G-T

90019794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79693964-G-A

90020216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79694299-A-G

90020475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79694528-G-A

http://identifiers.org/hco/15/GRCh38#90020490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79694543-C-A

90020490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79694543-C-G

90020490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79694543-C-T

90021000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695024-G-A

90021017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695035-C-G

90021017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695035-C-T

90021050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695068-G-A

90021069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695087-G-T

90021267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695223-A-G

90021360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695299-C-T

90021651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695534-C-G

90022451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79695867-G-A

90022665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79696047-A-T

90022667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79696049-A-G

http://identifiers.org/hco/15/GRCh38#90025177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79697220-C-A

http://identifiers.org/hco/15/GRCh38#90025331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79697366-C-A

90025331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79697366-C-T

90025459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79697478-G-A

90025459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79697478-G-T

90025522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79697526-A-G

http://identifiers.org/hco/15/GRCh38#90025726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79697717-C-A

90025923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79697928-A-G

90026023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698031-C-T

90026128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698132-G-A

http://identifiers.org/hco/15/GRCh38#90026147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79698149-C-A

90026147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698149-C-G

90026151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698153-C-T

90026168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698170-T-A

http://identifiers.org/hco/15/GRCh38#90026254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79698236-C-A

90026254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698236-C-T

90026290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698257-G-A

90026469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698441-A-G

90026493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698465-T-C

90026636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698606-T-A

90026735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698705-T-C

90026777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698750-G-A

90026777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79698750-G-T

90027847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79699557-A-G

90027857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79699567-A-G

90027955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79699665-A-T

90028605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79701660-A-G

90028887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79701904-G-A

90029110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702093-A-G

90029120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702103-C-T

90029330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702301-C-T

90029360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702330-G-A

90029444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702506-A-G

90029510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702569-T-G

90029586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702630-G-C

90029586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702630-G-T

90030406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79702815-G-C

90030704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703115-A-T

90031048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703335-A-G

90031055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703342-G-T

http://identifiers.org/hco/15/GRCh38#90031074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79703361-C-A

90031130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703389-G-A

90031174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, undefined
orthologous variants: 79703432-G-A

90031425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703652-G-T

90031557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703794-C-T

90031596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79703832-G-T

90032323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704416-G-A

90032368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704461-G-A

90032497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704870-G-A

90032510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704884-G-A

90032565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704943-G-A

90032566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79704944-T-C

90034503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79705902-T-C

90034731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706268-T-G

90035033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706475-C-T

90035156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706536-G-A

90035432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706720-C-T

90035519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706797-G-A

90035622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79706863-T-G

90035864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707104-C-G

90036303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707464-C-T

90036306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707467-A-G

90036343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707504-C-T

90036346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707507-T-C

90036350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707511-C-T

90036573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707714-T-A

90036707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79707856-C-T

90037321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79708575-C-T

90037459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79708691-C-T

90037651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79708830-T-G

90038006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709050-T-A

http://identifiers.org/hco/15/GRCh38#90038237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79709257-A-C

90038294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709314-G-A

http://identifiers.org/hco/15/GRCh38#90038644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79709535-C-A

90038709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709642-G-C

90038833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709790-C-G

90038833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709790-C-T

90038857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709806-A-G

90038874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79709823-C-T

90039822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79710351-A-G

90039919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79710424-A-G

90040012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79710508-G-A

90042346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712339-C-T

90042453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712429-C-G

90042453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712429-C-T

90042618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712595-A-G

90042770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712780-C-T

90042835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79712852-G-A

90043051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713098-G-A

http://identifiers.org/hco/15/GRCh38#90043107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79713178-A-C

90043302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713301-G-A

90043639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713558-G-T

90043730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713648-G-A

90043785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713700-G-A

90043838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713746-C-T

90043929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713840-T-C

90043930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713841-C-T

90044012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713914-G-A

90044136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79713998-A-T

90044179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714043-C-G

90044402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714233-C-G

90044402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714233-C-T

90044608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714426-G-C

90044656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714452-G-A

90044656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714452-G-T

90044886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714608-G-A

90045118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714795-G-T

90045183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714842-G-A

90045341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714972-G-A

90045341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714972-G-T

90045343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79714974-A-G

90045399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79715034-C-T

90045422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79715057-T-G

90045467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79715069-A-G

90045644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79715169-G-A

90045787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79715274-C-T

http://identifiers.org/hco/15/GRCh38#90046044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79715525-A-C

90046892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79716188-G-C

90046955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79716247-C-T

90047351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79716684-C-G

90049683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79719178-C-T

90049869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79719373-T-C

90049877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79719381-G-A

90050337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79719749-C-T

http://identifiers.org/hco/15/GRCh38#90050609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79719991-C-A

http://identifiers.org/hco/15/GRCh38#90050757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79720029-A-C

90052374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79721275-C-G

90054156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722122-G-A

90054244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722208-G-A

90054469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722408-G-T

90054649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722548-C-G

90054666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722556-G-T

90054692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722578-T-C

90055031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722895-G-C

90055041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79722896-G-A

90055404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79723368-C-T

90055673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79723540-G-A

90059648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79724714-G-A

90059688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79724727-G-A

90060053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79725056-T-C

90061121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79725392-G-T

90061122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79725393-G-C

90061905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79725780-T-G

http://identifiers.org/hco/15/GRCh38#90062160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79726034-A-C

90062160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79726034-A-T

90062161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79726035-C-T

http://identifiers.org/hco/15/GRCh38#90062817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79726675-C-A

90062817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79726675-C-G

90062817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79726675-C-T

90063110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79726794-C-T

90063464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727041-G-A

90063594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727130-G-A

90063655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727217-G-C

90064013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727708-C-T

90064058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727754-T-G

90064138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727835-G-A

90064162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79727861-C-T

90064390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79728234-G-A

90064856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79728384-G-A

90064856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79728384-G-C

90065016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79728519-G-A

90065384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79728845-C-T

90065474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79728962-T-G

90065486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79728974-G-A

90065486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79728974-G-C

90065902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79729327-T-A

90066033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79729450-C-T

http://identifiers.org/hco/15/GRCh38#90066137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79729558-A-C

90066473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79730096-G-A

http://identifiers.org/hco/15/GRCh38#90067012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79730706-C-A

http://identifiers.org/hco/15/GRCh38#90067329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731016-C-A

90067329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731016-C-T

http://identifiers.org/hco/15/GRCh38#90067347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731034-C-A

90067347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731034-C-T

http://identifiers.org/hco/15/GRCh38#90067353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731040-C-A

90067353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: 79731040-C-G

90067353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731040-C-T

90067356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731043-G-A

http://identifiers.org/hco/15/GRCh38#90067423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731110-C-A

90067423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: 79731110-C-T

90067581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731271-C-T

http://identifiers.org/hco/15/GRCh38#90067602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731292-C-A

90067602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731292-C-T

http://identifiers.org/hco/15/GRCh38#90067681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731371-C-A

http://identifiers.org/hco/15/GRCh38#90067813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79731503-C-A

90067813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: 79731503-C-G

90067855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: 79731548-G-T

90067911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731604-G-A

90067968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: missense variant
orthologous variants: 79731661-C-G

90067968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731661-C-T

90068109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731802-G-A

90068109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731802-G-C

90068169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731862-G-A

90068169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731862-G-C

90068259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731952-G-A

90068259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731952-G-C

90068289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731982-C-T

90068295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: synonymous variant
orthologous variants: 79731988-C-T

90068653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79732326-A-G

90068671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79732343-A-G

http://identifiers.org/hco/15/GRCh38#90068680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79732352-C-A

90068680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79732352-C-T

90069767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733614-C-G

http://identifiers.org/hco/15/GRCh38#90069851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79733698-C-A

90069851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733698-C-T

90069877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733728-T-C

90069998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733838-A-G

90070128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733929-A-T

90070140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79733950-G-T

90071129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79734040-T-C

90071134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79734045-G-A

http://identifiers.org/hco/15/GRCh38#90073301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79735907-A-C

90074072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron variant
orthologous variants: 79736142-G-C

90074397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79736463-T-G

90074592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736641-G-T

90074613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736659-G-A

90074613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736659-G-T

90074654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736689-G-A

90074654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736689-G-C

90074654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736689-G-T

90074732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79736761-T-C

90074949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736882-G-T

http://identifiers.org/hco/15/GRCh38#90074964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79736897-C-A

90074964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736897-C-T

90074993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736914-G-A

http://identifiers.org/hco/15/GRCh38#90075014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79736930-C-A

90075014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736930-C-T

90075052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736968-G-A

90075052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736968-G-T

90075060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736975-T-A

90075060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736975-T-C

90075060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79736975-T-G

http://identifiers.org/hco/15/GRCh38#90075126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737009-C-A

90075144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737021-G-A

90075243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737085-G-A

90075243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737085-G-T

http://identifiers.org/hco/15/GRCh38#90075246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737088-C-A

90075246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737088-C-T

http://identifiers.org/hco/15/GRCh38#90075258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737100-C-A

90075258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737100-C-T

http://identifiers.org/hco/15/GRCh38#90075444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737197-C-A

90075444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79737197-C-T

90075466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737219-G-A

http://identifiers.org/hco/15/GRCh38#90075480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737233-C-A

90075579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79737360-T-C

http://identifiers.org/hco/15/GRCh38#90075860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737613-C-A

90075860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737613-C-T

90075910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737638-T-G

http://identifiers.org/hco/15/GRCh38#90075928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737656-C-A

http://identifiers.org/hco/15/GRCh38#90075930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79737658-C-A

90078116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79738774-C-T

90078229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79738853-G-A

90078229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79738853-G-T

90078234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79738858-G-A

90078294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79738939-G-C

90078609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739182-G-T

90078918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739497-G-A

90079012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739628-G-A

90079148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739746-A-G

90079248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739828-G-T

90079519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739973-G-A

90079519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79739973-G-T

90079588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740022-G-A

http://identifiers.org/hco/15/GRCh38#90079589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79740023-C-A

90079589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740023-C-T

http://identifiers.org/hco/15/GRCh38#90079664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79740087-C-A

http://identifiers.org/hco/15/GRCh38#90079952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79740355-C-A

90079961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740373-T-A

90079961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740373-T-C

90080047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740459-G-A

90080047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740459-G-T

90080074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740485-A-G

http://identifiers.org/hco/15/GRCh38#90080172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79740588-C-A

90080433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740847-G-A

90080433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79740847-G-T

http://identifiers.org/hco/15/GRCh38#90080559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79740994-C-A

90080587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741020-G-A

90080587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741020-G-T

http://identifiers.org/hco/15/GRCh38#90080746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741198-C-A

90080746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741198-C-T

http://identifiers.org/hco/15/GRCh38#90080758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741218-C-A

90080758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741218-C-T

http://identifiers.org/hco/15/GRCh38#90080903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741383-C-A

90080942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741447-A-G

http://identifiers.org/hco/15/GRCh38#90081230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741635-C-A

90081233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741638-T-C

http://identifiers.org/hco/15/GRCh38#90081325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741674-C-A

http://identifiers.org/hco/15/GRCh38#90081333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741684-C-A

90081374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79741719-G-T

http://identifiers.org/hco/15/GRCh38#90081454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741800-C-A

90081454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79741800-C-G

http://identifiers.org/hco/15/GRCh38#90081471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741817-C-A

http://identifiers.org/hco/15/GRCh38#90081593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79741908-C-A

90081598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79741913-G-T

90081633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79741950-C-T

http://identifiers.org/hco/15/GRCh38#90081739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79742071-C-A