73065992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924507-T-C

73066096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924595-T-A

73066102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924599-G-A

73066140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924631-A-G

http://identifiers.org/hco/8/GRCh38#73066180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15924669-A-C

73066194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924683-A-G

73066213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924702-G-A

http://identifiers.org/hco/8/GRCh38#73066231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15924720-C-A

73066297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924786-G-A

http://identifiers.org/hco/8/GRCh38#73066298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15924787-C-A

73066298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924787-C-T

73066345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924848-T-C

73066387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924886-T-C

73066415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924913-G-A

73066415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924913-G-T

73066419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3 prime UTR variant
orthologous variants: 15924917-C-T

73066564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925031-G-T

73066643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925105-G-C

73066761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925214-T-C

73066853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925294-T-C

http://identifiers.org/hco/8/GRCh38#73067124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15925748-C-A

73067124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925748-C-G

73067124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925748-C-T

73067233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925859-G-T

73067237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925863-T-G

http://identifiers.org/hco/8/GRCh38#73067254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15925880-C-A

73067269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925897-A-G

73067327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15925955-A-G

http://identifiers.org/hco/8/GRCh38#73067397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15926025-C-A

73067481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15926109-T-C

http://identifiers.org/hco/8/GRCh38#73067513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15926141-C-A

http://identifiers.org/hco/8/GRCh38#73067522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15926150-A-C

73068311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15927445-T-C

73068379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15927512-G-T

73068529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15927645-T-G

73068549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15927663-T-A

73069588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15928918-C-G

73069668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15928996-G-T

http://identifiers.org/hco/8/GRCh38#73069706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15929022-C-A

73069706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929022-C-T

73069747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929063-G-A

73069747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929063-G-C

73069747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929063-G-T

73069762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929077-A-G

http://identifiers.org/hco/8/GRCh38#73069785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15929096-C-A

73069785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929096-C-G

73069785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929096-C-T

73069896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 15929204-G-A

73069896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15929204-G-C

73069996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929304-G-T

73069998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929306-A-G

73070002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929310-A-G

http://identifiers.org/hco/8/GRCh38#73070065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15929377-C-A

73070065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929377-C-T

73071310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929748-G-A

73071310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929748-G-T

73071379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929810-C-T

73071392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929823-T-C

73071474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15929996-C-T

73071547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930058-A-G

73071641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930146-G-T

73071658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930162-T-C

73071658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930162-T-G

73071668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930172-T-G

http://identifiers.org/hco/8/GRCh38#73071678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15930182-A-C

73071678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930182-A-G

73071689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930193-G-T

73071790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15930495-C-G

73071790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15930495-C-T

73071846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15930551-G-A

73071887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930592-T-A

http://identifiers.org/hco/8/GRCh38#73071951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15930654-C-A

73071951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930654-C-T

http://identifiers.org/hco/8/GRCh38#73071972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15930674-C-A

73071972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930674-C-G

73071972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930674-C-T

73072176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15930871-G-A

73072979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15931258-G-T

73072998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15931277-A-G

73073183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15931392-C-T

73075371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15947255-C-T

73075546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15947439-T-G

73075664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15947560-T-C

73076134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15947962-G-A

73076410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15948208-G-A

73076604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15948304-A-G

73076939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15948658-T-G

73077001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15948717-G-A

73077166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15948950-A-G

73078205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15950491-T-G

73078314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15950611-A-T

73078429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15950860-A-G

73078459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15950932-T-C

73078459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15950932-T-G

73078579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15951035-T-C

73078873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15951315-C-G

73078873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15951315-C-T

http://identifiers.org/hco/8/GRCh38#73079131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15951603-C-A

73079290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15951830-T-A

73079421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15951959-A-G

73079542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15952059-C-T

73079689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15952164-G-A

73079689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15952164-G-T

73079774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15952231-C-T

73079788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15952245-C-T

73079853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15952303-C-T

73079960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15952414-A-G

73080773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953613-T-A

73080773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953613-T-C

http://identifiers.org/hco/8/GRCh38#73080825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15953681-A-C

73080872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953729-G-T

http://identifiers.org/hco/8/GRCh38#73080920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15953777-C-A

73080920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953777-C-T

http://identifiers.org/hco/8/GRCh38#73080969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15953820-C-A

73080969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953820-C-G

http://identifiers.org/hco/8/GRCh38#73081013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15953864-C-A

73081013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15953864-C-T

73081228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954079-A-G

73081228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954079-A-T

http://identifiers.org/hco/8/GRCh38#73081235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15954086-C-A

73081235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954086-C-T

http://identifiers.org/hco/8/GRCh38#73081288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15954141-C-A

73081288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954141-C-T

73081302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954157-T-C

73081302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954157-T-G

http://identifiers.org/hco/8/GRCh38#73081325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15954182-C-A

73081325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954182-C-G

73081325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15954182-C-T

73082359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15956881-C-T

73082381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15956894-G-A

73082659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15957129-C-T

73082844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15957934-T-C

73083105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958185-G-T

73083203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958275-G-A

73087614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958540-T-C

73087625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958551-G-C

73087761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958658-G-A

73087950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15958860-G-A

73090212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959715-C-G

73090338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959844-A-G

73090378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959867-G-C

73090398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959891-T-A

73090420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959915-G-A

73090467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15959957-A-G

73090498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15959974-G-A

73090558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15960048-G-A

http://identifiers.org/hco/8/GRCh38#73090582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#15960070-C-A

73090588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15960076-T-G

73090639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15960123-G-A

73090857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15960325-G-A

73090857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15960325-G-C

73090870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15960337-C-T

73091501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15961493-A-G

73091636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15961625-T-C

73091726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15961694-T-C

73091730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15961698-C-T

http://identifiers.org/hco/8/GRCh38#73091731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15961699-A-C

73092171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962117-A-T

73092258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962180-T-C

73092402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15962301-A-G

73092556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962455-G-A

73092601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962494-G-A

73092729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962559-G-A

73092729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962559-G-T

73092814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962625-G-A

73092826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962635-G-A

73092925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15962734-C-T

73093080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15962889-G-A

73093080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15962889-G-C

73093080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15962889-G-T

73093108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15962922-G-A

73093108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15962922-G-C

73093108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15962922-G-T

http://identifiers.org/hco/8/GRCh38#73093138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15962952-C-A

73093138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15962952-C-G

73093138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15962952-C-T

http://identifiers.org/hco/8/GRCh38#73093221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15962994-C-A

73093221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15962994-C-T

73093355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963083-T-A

73093355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963083-T-C

http://identifiers.org/hco/8/GRCh38#73093370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15963095-A-C

73093370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963095-A-G

73093391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963116-C-T

73093598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15963247-C-G

73093610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963259-C-T

73093658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15963298-G-A

73094210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15964128-A-G

73094279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15964197-A-G

73094439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15964367-G-A

http://identifiers.org/hco/8/GRCh38#73094717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15964640-A-C

73095211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965412-G-A

73095267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965455-A-G

http://identifiers.org/hco/8/GRCh38#73095274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15965462-C-A

73095274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965462-C-T

73095422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965584-G-C

73095465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965610-A-G

73095504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965649-A-T

73095616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965746-C-T

73095743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965842-A-G

http://identifiers.org/hco/8/GRCh38#73095752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15965851-A-C

73096099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15965889-T-C

73096898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15966536-C-T

73099946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15969983-T-C

http://identifiers.org/hco/8/GRCh38#73100009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15970043-A-C

73100135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15970173-G-A

http://identifiers.org/hco/8/GRCh38#73100194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15970238-C-A

73100554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15970578-G-A

73100570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15970594-T-G

73100685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15970746-G-A

73100746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15970800-T-C

73101665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972354-A-G

73101756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972573-C-T

73101812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972622-A-G

73101892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972686-T-C

73101906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972700-A-G

73101920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972715-C-T

73101941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972736-G-A

73102235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15972974-C-T

73102279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973017-T-C

73102280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973018-A-G

73102503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973288-C-G

73102621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973374-G-T

73102646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973392-G-A

73102727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15973461-C-T

73103877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975262-C-T

http://identifiers.org/hco/8/GRCh38#73103882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15975267-C-A

73103939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975324-G-A

73103964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975349-G-T

73104177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975549-T-G

73104349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975733-T-C

73104444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975836-T-G

73104449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975841-A-G

73104479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15975868-G-A

73105498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976730-T-C

73105589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976795-C-T

73105626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976828-G-A

73105626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976828-G-C

73105729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976904-G-A

73105779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15976957-G-T

73105793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977020-C-G

73105801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977062-A-G

73105869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977135-G-A

73105869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977135-G-C

73105893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977144-G-A

73105893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977144-G-C

73105905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977153-G-A

73105949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977190-G-A

73106016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977249-G-A

73106169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977391-T-C

73106244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977468-G-T

http://identifiers.org/hco/8/GRCh38#73106350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15977555-C-A

73106350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977555-C-T

73106415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15977616-T-C

73106451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15977641-A-G

73106482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15977670-C-T

73106531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15977687-G-A

73106635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977720-C-T

73106671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977751-C-T

73106702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977785-A-G

73106840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15977884-A-G

http://identifiers.org/hco/8/GRCh38#73106926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15978158-A-C

73106963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978195-G-A

73106963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978195-G-C

73106963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978195-G-T

73107028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978258-G-A

73107260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978666-G-A

73107260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978666-G-C

73107374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978819-G-C

73107525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15978993-A-G

73107572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979037-G-T

73107713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979171-A-G

73107865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979268-C-T

73107902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979306-A-G

73107914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979318-T-A

http://identifiers.org/hco/8/GRCh38#73107931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15979346-C-A

73107959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979369-G-A

http://identifiers.org/hco/8/GRCh38#73107968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15979371-C-A

73107968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979371-C-T

73108013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979416-C-T

73108101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979503-T-A

http://identifiers.org/hco/8/GRCh38#73108109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15979518-A-C

73108114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979523-C-T

73108146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979560-G-T

http://identifiers.org/hco/8/GRCh38#73108175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15979591-C-A

73108184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979596-T-C

73108206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15979610-G-T

73108286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15979703-G-T

http://identifiers.org/hco/8/GRCh38#73108450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15979891-C-A

http://identifiers.org/hco/8/GRCh38#73109491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15980263-C-A

73109789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15980564-C-T

73109996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15980762-A-G

73110071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15980829-T-C

73110076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15980834-A-G

73111086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983110-G-T

73111103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983127-C-T

73111224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983227-A-G

http://identifiers.org/hco/8/GRCh38#73111229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15983232-C-A

73111393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983372-A-T

73111567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983495-G-T

73111600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983526-A-G

73111640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983568-T-A

73112012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983896-C-T

73112063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15983946-G-A

73112230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15984507-A-G

http://identifiers.org/hco/8/GRCh38#73112241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15984518-A-C

73113619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985388-G-A

73113619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985388-G-C

73114031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985879-A-G

73114036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985884-T-C

73114065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985913-A-T

73114077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985926-A-G

73114212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15985990-C-T

73114332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15986109-C-T

73116646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15987639-A-G

73116656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15987649-G-A

73116734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15987723-A-G

73116942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15990942-G-A

73116942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15990942-G-T

73116976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15990974-T-C

73117079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991038-C-T

73117336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992196-G-A

73117457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992303-G-C

73117824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991282-G-C

73117938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991387-G-A

73117938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991387-G-T

73117944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991393-C-T

73118070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991528-C-T

73118110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991547-G-A

73118125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991567-G-C

73118134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991576-G-A

73118535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15991927-A-G

73118765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992149-T-C

73118768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992153-C-T

73118863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992246-G-C

73119138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992483-C-T

73119159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15992500-G-A

73119672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15994206-G-A

73119961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15994736-T-C

73120151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15994921-G-C

73120178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15994963-C-T

73120235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15995016-C-T

http://identifiers.org/hco/8/GRCh38#73120237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#15995018-C-A

73120297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15995070-C-T

73120331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15995102-A-G

73120336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15995107-C-T

73120404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15995173-A-G

73120601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996207-G-A

73120798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996403-C-G

73120798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996403-C-T

73120832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996437-C-G

73120919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996524-G-A

73121227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15996846-T-C