http://identifiers.org/hco/15/GRCh38#89361771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79149074-C-A

89361771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149074-C-G

89361771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149074-C-T

89361788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149091-C-T

89361812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149114-A-G

89361812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149114-A-T

89361827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149128-G-A

http://identifiers.org/hco/15/GRCh38#89361926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79149227-C-A

89361926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 79149227-C-T

89362270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 79149557-G-T

89362289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149576-G-T

89362290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149577-A-G

89362325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149585-G-A

89362338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149601-G-A

89362338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149601-G-T

89362547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149811-T-C

89362604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79149868-G-A

89362823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150086-G-A

89362856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150118-G-A

89362856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150118-G-T

http://identifiers.org/hco/15/GRCh38#89362871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79150133-C-A

89362871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150133-C-T

89362919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150180-G-A

89362966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150221-C-G

89362966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150221-C-T

89362995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150269-A-G

89363217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150501-A-T

http://identifiers.org/hco/15/GRCh38#89363311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79150594-A-C

89363311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150594-A-G

89363313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150596-T-C

http://identifiers.org/hco/15/GRCh38#89363605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79150872-C-A

89363605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150872-C-T

89363617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150884-C-T

89363653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79150926-G-A

89363856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151086-G-T

89364115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151348-G-T

http://identifiers.org/hco/15/GRCh38#89364303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79151518-A-C

89364697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151847-G-A

89364753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151886-G-A

89364755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151887-G-A

89364755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151887-G-C

89364778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79151920-T-C

89364999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79152140-A-G

http://identifiers.org/hco/15/GRCh38#89365001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79152142-C-A

89365001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152142-C-T

89365086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152199-C-T

89365097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152210-G-T

http://identifiers.org/hco/15/GRCh38#89365391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79152447-A-C

89365405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152464-C-T

89365648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152705-G-A

89365648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79152705-G-T

89366456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79153547-A-T

89366518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79153608-G-A

89366549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79153641-T-C

http://identifiers.org/hco/15/GRCh38#89366761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79153848-C-A

89366812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79153897-G-T

89366921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79153996-G-A

89367193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79154236-C-T

89367518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79154536-G-C

89367697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79154715-G-C

89367734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79154752-C-T

89367804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79154808-G-T

89368169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79155154-G-A

89368169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79155154-G-T

89368547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79155642-T-G

89368552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79155647-T-G

89368955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79156049-G-A

89368996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79156091-A-G

http://identifiers.org/hco/15/GRCh38#89369147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79156245-C-A

http://identifiers.org/hco/15/GRCh38#89369264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79156370-C-A

89369361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79156466-G-A

http://identifiers.org/hco/15/GRCh38#89369449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79156564-C-A

89369449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79156564-C-T

89369930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79157037-G-A

89371450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79158482-G-A

89371450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79158482-G-T

89371678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79158656-G-A

89371903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79158884-A-G

89372549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79159472-G-T

89373045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79159954-T-C

89373057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79159966-C-T

89374086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79160989-G-A

89375030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79161908-G-A

89375516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79162353-A-G

89375751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

89376138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79162985-G-A

89376193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163079-T-G

http://identifiers.org/hco/15/GRCh38#89376321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79163126-C-A

89376321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163126-C-T

89376322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163127-T-C

http://identifiers.org/hco/15/GRCh38#89376926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79163614-C-A

89376942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163628-G-T

89377028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163723-G-C

89377045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163740-C-T

89377166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79163861-G-A

89377347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164058-T-G

89377471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164170-G-A

89377522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164194-G-A

89377800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79164337-G-A

89377800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79164337-G-C

http://identifiers.org/hco/15/GRCh38#89377900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79164407-C-A

89377900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164407-C-T

89377973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79164478-C-G

89377977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79164482-A-G

89377977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79164482-A-T

89378011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79164515-G-T

http://identifiers.org/hco/15/GRCh38#89378076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79164578-C-A

89378076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79164578-C-T

http://identifiers.org/hco/15/GRCh38#89378115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79164621-C-A

89378149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79164639-G-A

89378149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79164639-G-T

http://identifiers.org/hco/15/GRCh38#89378250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79164753-C-A

89378250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79164753-C-G

89378250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79164753-C-T

89378270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79164773-T-C

89378311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164814-G-A

89378311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79164814-G-T

89378537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79165049-G-A

89378537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79165049-G-C

89378537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79165049-G-T

89378681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165135-C-T

89378837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165254-G-A

89378837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165254-G-T

89378913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165337-T-C

89378914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165338-G-A

89379108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165535-G-A

89379233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165614-G-A

89379243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165624-T-C

89379243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165624-T-G

89379298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165683-C-T

89379345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165746-G-A

89379345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79165746-G-C

89379372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165798-G-A

89379372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165798-G-C

89379372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79165798-G-T

89379411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79165832-C-T

89379413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79165834-T-C

http://identifiers.org/hco/15/GRCh38#89379485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79165905-C-A

89379779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79166180-C-T

89379811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79166212-C-T

89379831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79166226-A-G

89380061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79166421-G-T

89380304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79166659-A-G

89380443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79166877-G-A

89380482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79166914-A-G

http://identifiers.org/hco/15/GRCh38#89380615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79167043-A-C

89381083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79167508-C-T

89381179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79167598-C-T

http://identifiers.org/hco/15/GRCh38#89382503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79168897-C-A

89382503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79168897-C-T

http://identifiers.org/hco/15/GRCh38#89382552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79168946-C-A

89383206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79169579-T-A

89383731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79170052-C-T

89383876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79170204-A-G

89384283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79170568-G-A

89384283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79170568-G-C

89385731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79171970-C-G

89386922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79172767-A-G

89387014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79172829-T-C

89387015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79172830-G-A

89387116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79172944-G-T

89387133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79172961-G-T

89387175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173034-A-T

89387302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173168-G-A

89387302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173168-G-T

89387344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173210-T-C

89387356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173222-A-G

89387367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173233-A-G

89387394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173256-G-T

89387819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79173667-C-G

89387819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79173667-C-T

89387869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173750-C-G

89387869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173750-C-T

89387977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173850-G-T

89388043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79173910-G-T

http://identifiers.org/hco/15/GRCh38#89388101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79173970-C-A

http://identifiers.org/hco/15/GRCh38#89388123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79173994-C-A

89388123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79173994-C-T

89388482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 79174278-A-G

http://identifiers.org/hco/15/GRCh38#89388823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79174641-C-A

89388832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174650-T-C

http://identifiers.org/hco/15/GRCh38#89388834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79174652-C-A

89388835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174653-A-T

89388885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174689-C-T

89388977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174778-C-T

89389031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174832-C-T

89389197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174989-G-A

89389197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79174989-G-T

89389220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79175012-G-T

http://identifiers.org/hco/15/GRCh38#89389318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79175103-C-A

89389318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79175103-C-T

89389389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79175174-G-A

89389402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79175187-C-T

89389529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79175315-T-C

http://identifiers.org/hco/15/GRCh38#89389609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79175433-C-A

89389609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79175433-C-T

89389614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79175438-G-A

89389614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79175438-G-T

http://identifiers.org/hco/15/GRCh38#89389620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79175443-C-A

89390208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176044-G-A

89390208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176044-G-T

89390448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176277-T-C

89390865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176638-G-T

89391002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176785-C-T

89391099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176852-C-G

89391099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176852-C-T

89391129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79176882-T-G

89391744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79177774-T-C

89392059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178090-C-T

89392127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178158-G-A

89392127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178158-G-C

89392155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178186-G-A

89392457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178395-G-T

89392541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178466-G-A

89392541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178466-G-C

89392659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79178576-C-T

89393313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79179336-G-A

89393350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79179377-T-A

89393413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79179428-C-T

89394328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180032-C-T

http://identifiers.org/hco/15/GRCh38#89394356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79180051-C-A

89394356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180051-C-T

89394793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180713-G-A

http://identifiers.org/hco/15/GRCh38#89394981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79180883-C-A

89394987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180894-A-G

89394992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180899-G-A

89394992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180899-G-T

89394997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180903-G-A

89394997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79180903-G-T

http://identifiers.org/hco/15/GRCh38#89395229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79181106-C-A

89395280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181133-G-T

http://identifiers.org/hco/15/GRCh38#89395289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79181142-C-A

89395330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181180-T-A

89395334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181184-T-G

89395349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181199-G-A

89395349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181199-G-C

89395349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181199-G-T

http://identifiers.org/hco/15/GRCh38#89395380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79181224-C-A

89395473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181323-G-A

89395473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181323-G-T

http://identifiers.org/hco/15/GRCh38#89395522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79181369-C-A

89395522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181369-C-G

89395522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181369-C-T

89395687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181533-A-G

89395717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181563-G-A

89395717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181563-G-T

89395775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181622-G-T

89395987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181829-G-A

89395987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79181829-G-T

89396162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182010-C-G

89396272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182065-C-T

89396753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182561-G-A

89396753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182561-G-T

89397036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182849-G-A

89397036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182849-G-T

89397252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79182984-A-G

http://identifiers.org/hco/15/GRCh38#89397365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79183104-C-A

89397367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183106-G-T

89397379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183113-G-T

89397456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183185-G-A

89397541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183242-G-T

89397554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183254-A-G

89397595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183281-T-C

89397620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183306-G-A

89397620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183306-G-C

89397620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183306-G-T

89397621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183307-G-A

89397621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183307-G-T

89397729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183378-T-C

89397731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183380-T-C

89397979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183609-A-T

89398161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183776-G-T

89398181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183835-G-T

89398306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183970-G-C

89398307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183971-G-A

89398307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79183971-G-T

89398383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79184040-G-T

89398460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79184127-T-C

http://identifiers.org/hco/15/GRCh38#89398628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79184278-C-A

89398628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184278-C-T

89398779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184406-C-T

89398797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184424-A-G

89398966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184564-G-C

89399065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79184670-G-C

89399397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79185014-G-A

89399744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79185370-G-A

89399784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79185397-C-T

89399889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79185503-G-T

89400001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79185586-G-A

http://identifiers.org/hco/15/GRCh38#89400140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79185732-A-C

89400217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79185804-C-G

89400606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79186161-G-A

89401045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79186497-C-T

89401831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79187204-C-T

89404833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190713-C-T

89404879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190757-A-T

89404880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190758-G-A

89404939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190823-T-G

89405010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190899-A-G

http://identifiers.org/hco/15/GRCh38#89405056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79190945-C-A

89405056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190945-C-T

89405085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79190994-G-C

89405162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191047-T-C

89405618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191415-C-T

89405717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191512-G-T

89405870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191625-G-A

http://identifiers.org/hco/15/GRCh38#89405898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79191645-C-A

89405942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191691-T-C

89405965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79191713-T-A

http://identifiers.org/hco/15/GRCh38#89406292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79192193-C-A

89406387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192286-G-A

89406427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192324-A-T

89406766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192657-G-T

89406775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192666-G-C

89406825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192704-G-A

89406893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192801-C-T

89407051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79192960-T-G

http://identifiers.org/hco/15/GRCh38#89407405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79193282-C-A

89407454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79193315-C-G

http://identifiers.org/hco/15/GRCh38#89407578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79193437-C-A

89407578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79193437-C-G

89407578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79193437-C-T

89407608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79193467-G-A

89407746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79193605-C-T

89407803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79193643-G-T

89408049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79193890-C-G

89408157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194048-C-T

89408311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194211-G-T

89408500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194393-C-T

89408642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194527-G-A

89408930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194802-C-T

89408939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194811-G-A

89408939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194811-G-C

89408939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194811-G-T

89409015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194904-T-A

89409022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194911-G-C

89409073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194961-T-C

89409073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79194961-T-G

http://identifiers.org/hco/15/GRCh38#89409497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79195385-A-C

89409957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79195612-C-G

89410128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79195767-C-T

http://identifiers.org/hco/15/GRCh38#89410203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79195819-C-A

89410233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79195851-C-T

http://identifiers.org/hco/15/GRCh38#89410391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79196023-A-C

http://identifiers.org/hco/15/GRCh38#89410517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79196127-C-A

89410564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79196158-C-T

89410565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79196159-G-A

89411056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79196499-G-C

http://identifiers.org/hco/15/GRCh38#89411342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79196741-C-A

89411431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196823-G-A

89411431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196823-G-T

89411461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196837-C-G

89411461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196837-C-T

89411597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196972-G-A

89411597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196972-G-T

89411630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79196993-G-A

89411911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79197237-C-T

89412104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79197618-G-A

89412234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79197797-G-A

89412309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79197912-T-C

89412591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79198352-G-T

89412607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79198381-A-G

89412765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79198550-C-G

http://identifiers.org/hco/15/GRCh38#89413024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79198754-C-A

89413024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79198754-C-T

89413696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199443-C-T

89413730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199479-C-T

89413795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199544-C-G

89413795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199544-C-T

89413814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199566-A-T

89413910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199655-T-C

89413945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79199690-G-C

89415245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79200543-C-T

89415420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79200669-C-G

89415420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79200669-C-T

89415757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79201388-C-T

89416210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79202039-G-A

89416299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79202122-G-A

89416413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79202440-T-C

89416435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202581-G-A

89416480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202632-A-T

89416507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202653-T-C

89416513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202661-G-A

89416714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202831-G-T

89416743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202856-T-C

89416899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79202979-C-G

89417104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79203137-G-A

89417112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79203145-G-A

89417140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79203173-G-A

89417331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79203355-T-C

89417533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79203586-C-G

89417587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79203634-G-C

89417872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79203889-A-G

89418013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79204144-G-A

89418120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79204273-G-A

89418338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79204443-T-G

http://identifiers.org/hco/15/GRCh38#89418479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79204545-A-C

89419063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79205117-C-T

89419350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79205345-C-G

89419350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79205345-C-T

89419390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79205415-G-A

89419390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79205415-G-T

89419526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79205556-A-G

89419703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79205682-G-T

89419756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79205732-C-T

89423530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79207074-T-C

http://identifiers.org/hco/15/GRCh38#89423608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79207144-C-A

89423621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79207164-A-G

89423764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79207280-A-T

89423854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79207369-C-T

89424110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79207563-C-T

89424502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79207932-C-T

http://identifiers.org/hco/15/GRCh38#89424561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79207981-C-A

89424571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79207991-T-G

http://identifiers.org/hco/15/GRCh38#89424585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79208029-C-A

89424587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79208031-G-A

89424587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79208031-G-T

http://identifiers.org/hco/15/GRCh38#89424882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79208284-A-C

89424882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79208284-A-G

89424882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79208284-A-T

89424887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27388
most severe consequence: non coding transcript exon variant
orthologous variants: 79208295-G-T