http://identifiers.org/hco/15/GRCh38#80679718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83826767-C-A

80679718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 83826767-C-T

80679785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826708-C-T

80679787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826706-C-G

80679787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826706-C-T

80679798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826695-T-A

80679813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83826680-C-T

80679890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826613-T-C

80679903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83826600-T-G

80680023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826486-G-T

80680052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826469-G-A

80680083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83826460-G-A

80680274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83826301-G-C

80680298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83826264-A-G

80681768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83824260-A-G

http://identifiers.org/hco/15/GRCh38#80682281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83823887-A-C

80682709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83823286-G-A

80682709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83823286-G-T

http://identifiers.org/hco/15/GRCh38#80682735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83823260-A-C

80682804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83823205-G-C

http://identifiers.org/hco/15/GRCh38#80682852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83823177-A-C

80682853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83823176-A-G

80682926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83823082-A-G

80683135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83822917-G-A

80683135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83822917-G-T

80683332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83822730-A-G

80684740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83821827-A-G

80685012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83821321-A-G

80685074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83821260-T-G

80685119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83821216-T-A

http://identifiers.org/hco/15/GRCh38#80685378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83821044-A-C

80685378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83821044-A-G

http://identifiers.org/hco/15/GRCh38#80685807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83820703-A-C

80685970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83820595-G-A

80685998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83820567-G-A

80686115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83820481-C-G

80686478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: -T-C

80686554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: -T-C

80689301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83816030-C-T

80689360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815878-T-A

80689395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815838-T-C

80689499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815753-C-G

80689644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815596-G-A

80689854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815406-T-C

80689868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815392-A-G

80689912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83815374-G-A

80691787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803846-G-A

80691787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803846-G-C

80692776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803163-A-G

80692862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803082-G-A

80692862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803082-G-C

80692862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803082-G-T

80692863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803081-G-T

80692884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83803056-T-C

80692957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83802993-C-T

80693454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83802789-T-C

http://identifiers.org/hco/15/GRCh38#80693562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83802698-C-A

80693562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83802698-C-T

http://identifiers.org/hco/15/GRCh38#80693818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83802519-C-A

80693818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83802519-C-T

80694424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83801978-G-C

80694431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801971-C-T

80694433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801969-A-T

80694489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801919-T-C

80694818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801566-G-C

80694831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801553-C-T

80694904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801490-T-C

80694990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83801385-C-T

80695000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83801375-C-T

80695039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83801342-G-A

80695039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83801342-G-T

80695250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83801163-C-T

80696084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83800453-G-A

80696084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, undefined
orthologous variants: 83800453-G-T

80696584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83800069-A-G

80696753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799924-T-A

80696758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799919-G-T

80696801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799880-T-G

80697044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799656-A-G

80697177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799522-G-A

80697215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799484-C-G

80697238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799464-C-G

80697312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83799390-A-T

80697673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83798799-G-A

80698552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83798141-G-A

80698552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83798141-G-T

80698574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83798119-G-A

80699437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796933-A-G

http://identifiers.org/hco/15/GRCh38#80699500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83796870-A-C

80699543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796831-A-G

80700025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796475-A-T

80700069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796434-A-G

80700089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796414-C-G

80700193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83796332-T-G

80701322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron variant
orthologous variants: 83795706-A-G

80702725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794664-G-T

http://identifiers.org/hco/15/GRCh38#80702726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83794663-C-A

80702727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794662-T-C

http://identifiers.org/hco/15/GRCh38#80702939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83794491-C-A

80702939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794491-C-T

80702950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794481-C-T

http://identifiers.org/hco/15/GRCh38#80702977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83794449-C-A

80702977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794449-C-T

80703141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794297-G-A

80703141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83794297-G-T

http://identifiers.org/hco/15/GRCh38#80703142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83794296-C-A

80704845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83793843-G-T

http://identifiers.org/hco/15/GRCh38#80704870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83793813-C-A

80704870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83793813-C-T

80704936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83793741-A-G

80705128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83793600-T-C

80705299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83793437-G-T

80705300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83793436-A-T

80705820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83792985-A-G

80706110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83792722-C-T

80706471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83792392-G-A

80706471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83792392-G-T

80706946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83791895-A-T

80706972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83791868-G-A

80711418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788817-C-T

80711460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788782-G-T

80711487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788760-G-A

http://identifiers.org/hco/15/GRCh38#80711518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83788733-A-C

80711518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788733-A-T

80711552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788699-A-G

80711994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788295-T-A

http://identifiers.org/hco/15/GRCh38#80712214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83788085-C-A

80712214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788085-C-T

80712241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83788028-C-T

80712302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83787969-G-T

80712465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83787804-C-T

80712545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83787735-C-G

80712545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83787735-C-T

80713071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83787294-A-G

80714355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786826-T-C

80714515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786667-G-A

80714515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786667-G-T

80714696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786489-G-T

80714709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786476-T-A

80714910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83786339-T-C

80715718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785834-G-T

http://identifiers.org/hco/15/GRCh38#80715719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83785833-C-A

80715719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785833-C-T

80715744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785797-G-A

80716017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785557-A-T

80716056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785527-G-A

80716095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785471-G-T

http://identifiers.org/hco/15/GRCh38#80716103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83785463-A-C

80724804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780196-G-T

80726851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778580-G-A

80726866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778565-G-A

80726907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778528-T-C

80726959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778489-G-C

80727105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778363-C-T

80727106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778362-T-G

80727274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778227-G-A

80727274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778227-G-T

80727422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778084-G-A

80727422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778084-G-T

80727494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778021-A-G

80727720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777872-G-T

80727817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777785-T-C

80727911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777690-C-G

80728219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777463-A-G

http://identifiers.org/hco/15/GRCh38#80728303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83777404-C-A

80728303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777404-C-T

80728582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777207-A-T

80728900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777010-C-T

80728973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83776976-G-A

80729088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83776874-T-G

80729475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83776643-A-G

80729700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83776445-G-A

80729766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83776381-G-A

80731036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83775280-C-T

80731050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83775266-G-A

80731198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83775128-T-G

80731836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83774402-G-C

80732309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773538-G-A

80732345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773500-T-C

80732577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773271-G-A

80732577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773271-G-C

80732577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773271-G-T

80733638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

80733700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771962-A-G

http://identifiers.org/hco/15/GRCh38#80733716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83771946-A-C

80733853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771829-A-G

80734380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771594-G-A

80734380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771594-G-T

80734387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771587-G-A

80735018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771055-C-T

http://identifiers.org/hco/15/GRCh38#80735101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

80735101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

80735241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770133-T-C

80735401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769982-C-T

80735534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769848-T-G

80735858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769580-A-T

80736028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769270-G-A

http://identifiers.org/hco/15/GRCh38#80736196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83769118-C-A

80736196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769118-C-T

80736202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769113-A-G

80736212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769103-G-T

80736264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769053-C-T

80736449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768916-G-A

80737228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768267-T-C

80737248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768247-G-A

80737291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768213-A-G

80737361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768132-A-T

80737586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767648-G-C

80737586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767648-G-T

80737606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767629-G-A

80737617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767618-A-G

http://identifiers.org/hco/15/GRCh38#80737645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83767586-C-A

80737721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767511-C-T

80738085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767287-A-G

80738098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767274-G-C

80738260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767133-T-C

80738275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83767119-C-T

80738711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83766707-C-T

80739036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83766457-A-G

80739901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83766149-G-A

80739901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83766149-G-T

80740089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83765981-T-A

80740272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83765794-T-A

80748467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764586-T-G

80748532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764532-C-T

80748608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764428-C-G

80748608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764428-C-T

80748683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764355-A-T

80748837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764224-G-A

80748899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764187-C-G

80748912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764175-C-T

80749011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764074-A-G

80749399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763741-T-C

http://identifiers.org/hco/15/GRCh38#80749728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83763424-C-A

80749737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763421-G-A

80749760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763398-A-T

80749785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763377-A-G

80749820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763348-C-T

80749823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763345-G-T

80749826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763342-A-G

80749826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763342-A-T

80749836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763333-A-G

80749836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83763333-A-T

80750166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763031-G-C

http://identifiers.org/hco/15/GRCh38#80750293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83762885-C-A

http://identifiers.org/hco/15/GRCh38#80750387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83762724-C-A

80750387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83762724-C-T

80750895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83762291-G-T

80751865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83761994-T-C

80752686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83761214-G-A

80752970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760951-G-A

http://identifiers.org/hco/15/GRCh38#80753218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83760567-A-C

80753218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760567-A-G

80753251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760534-T-A

80753826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760190-C-T

80754089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760066-G-A

80754376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83759782-A-G

80754529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83759636-A-G

80754705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83759468-C-T

80755187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83759015-G-A

80755187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83759015-G-T

80755333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83758870-A-G

80755582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26925
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83758601-A-T