http://identifiers.org/hco/3/GRCh38#86883143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65747088-C-A

86883201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65747040-G-T

86883260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65746997-T-G

86883331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65746945-A-G

86883651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65746622-G-A

86889386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741651-C-T

86889396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

86889556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741507-C-G

86889728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741351-A-G

86889738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741341-T-C

86889803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741260-C-T

http://identifiers.org/hco/3/GRCh38#86889828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65741236-C-A

86889828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741236-C-G

86889849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741211-T-C

86889882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65741157-C-T

86890172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65740903-A-G

86890576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65739243-G-C

http://identifiers.org/hco/3/GRCh38#86890674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65739154-C-A

86890772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65739053-T-C

http://identifiers.org/hco/3/GRCh38#86890773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65739052-C-A

86890773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65739052-C-T

86890802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65739023-G-A

86890802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65739023-G-T

86891170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738658-A-G

86891175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738653-G-A

86891175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738653-G-T

86891302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738523-T-C

86891370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738457-A-G

86891447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738366-T-G

86891528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65738286-T-C

86892492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65736816-T-A

86892492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65736816-T-C

http://identifiers.org/hco/3/GRCh38#86893222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65724040-C-A

86893374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65722747-T-C

86893484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65722638-T-C

86893500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65722622-C-G

86893508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65722614-A-G

http://identifiers.org/hco/3/GRCh38#86893524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65722598-A-C

86894569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65721587-A-G

86894707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65721461-A-G

86894729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65721439-T-G

86894943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65721254-G-T

86895030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65721147-A-T

86896702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720717-A-G

86896727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720693-G-C

86896946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720498-C-T

86897541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720032-C-T

86897542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720031-G-A

86897560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720013-G-C

86897562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65720011-G-T

86898277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65719603-A-T

86898478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65719392-A-G

86898796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65719096-G-T

86898848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65719052-T-G

86898875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65719023-T-C

86898937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65718963-T-A

86899323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65718894-C-G

86899338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65718880-G-A

86899419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65718794-G-A

http://identifiers.org/hco/3/GRCh38#86899870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65714288-A-C

86899882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65714276-A-G

http://identifiers.org/hco/3/GRCh38#86899929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65714229-A-C

86899929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65714229-A-T

86899977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65714185-G-A

86900362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65713872-A-G

86900498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65713736-T-C

86900656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65713590-T-C

86900764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65713467-C-T

86901890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65706395-C-T

86902180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65706118-T-C

86904293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65705178-G-A

86904407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65705055-T-C

86904686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704780-C-T

86904716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704753-A-G

86904798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704713-A-G

http://identifiers.org/hco/3/GRCh38#86904874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65704651-C-A

86904874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704651-C-T

86904951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704573-A-G

http://identifiers.org/hco/3/GRCh38#86905318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65704214-A-C

86905421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704113-G-T

86905441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704101-G-A

86905469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704073-T-C

86905489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704053-T-G

86905531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65704010-T-C

86908523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703710-T-C

86908523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703710-T-G

86908529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703704-A-G

86908544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703689-T-C

86908566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703667-G-A

86908566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703667-G-C

86908566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 65703667-G-T

86908922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65703336-T-C

86908957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65703310-G-A

86908957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65703310-G-T

86909136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65703016-A-G

86909192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702887-T-C

86909594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702489-T-C

86909594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702489-T-G

86909606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702476-T-C

86909613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702469-C-T

86909969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702115-A-G

86910073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65702015-G-C

http://identifiers.org/hco/3/GRCh38#86910106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65701980-A-C

86910215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701872-T-C

86910363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701718-A-G

86910442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701639-A-G

86910488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701584-T-G

86910505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701567-T-C

86910522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65701549-A-G

86911865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65700119-C-T

86911890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65700096-G-A

86912041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699950-C-T

86912647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699641-G-A

86912647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699641-G-T

86912649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699639-A-G

http://identifiers.org/hco/3/GRCh38#86912750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65699558-C-A

86912768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699542-T-A

86912847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65699464-C-G

86917091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65698026-A-G

86917127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697990-A-G

86917172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697946-C-T

86917244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697874-C-T

86917266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697851-T-G

86917286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697837-T-G

http://identifiers.org/hco/3/GRCh38#86917385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65697740-A-C

86917385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697740-A-T

86917404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697721-A-T

86917481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697650-A-G

86917517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697614-T-A

86917538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697596-T-C

86917702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697462-G-A

86917721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697444-G-T

86917747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697418-A-G

86917757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697408-C-T

86918034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697164-A-G

86918065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697136-G-T

86918199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65697011-A-G

86918264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65696951-C-T

86918328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65696902-C-G

86921847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687540-A-G

86921847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687540-A-T

86921900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687480-G-C

86921913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687467-C-T

86921923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687457-G-A

86921936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687442-T-C

86921979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687389-C-T

86921993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687375-T-C

86922106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687259-G-A

86922174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687191-G-C

86922238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65687122-T-C

http://identifiers.org/hco/3/GRCh38#86922240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65687120-C-A

86922440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686943-T-G

86922522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686862-G-T

86922587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686802-G-A

86922587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686802-G-C

http://identifiers.org/hco/3/GRCh38#86922590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65686799-C-A

86922590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686799-C-G

http://identifiers.org/hco/3/GRCh38#86922617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65686775-A-C

86922723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686673-T-A

86922788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686622-G-A

86922853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686569-G-A

86922892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686520-C-T

86922959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686458-T-C

86922962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686446-A-T

86923034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686382-G-C

http://identifiers.org/hco/3/GRCh38#86923079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65686340-A-C

86923079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686340-A-G

86923366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65686072-T-C

86923543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685881-C-T

86923546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685878-T-C

86923596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685823-T-G

86923616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685803-T-A

86923616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685803-T-C

86923713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685703-G-A

http://identifiers.org/hco/3/GRCh38#86923839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65685580-C-A

86923839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685580-C-T

http://identifiers.org/hco/3/GRCh38#86923905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65685519-C-A

86923940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65685484-A-G

86925435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679594-A-G

86925444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679585-G-A

86925482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679547-G-A

86925482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679547-G-T

86925492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679537-T-C

http://identifiers.org/hco/3/GRCh38#86925656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65679408-A-C

86925677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679386-G-C

86925681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679382-T-C

86925749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679323-C-T

86925779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679293-C-G

86925808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65679275-G-T

86925961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65674081-C-T

86926201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673845-A-G

86926279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673763-G-T

86926380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673672-C-G

86926380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673672-C-T

86926602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673502-A-G

86926765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673363-A-T

86926804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673324-C-T

86926970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673170-G-A

86927021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65673140-T-G

86927225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672941-C-G

86927387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672787-G-A

86927482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672736-C-G

86927768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672512-A-G

86927881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672406-A-G

86927912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672370-T-C

86928011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672268-T-C

86928018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65672261-A-T

86928227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671959-G-A

86928344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671869-G-A

86928424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671800-A-G

86928455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671771-A-T

http://identifiers.org/hco/3/GRCh38#86928495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65671748-C-A

86928529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671714-A-T

86928533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671710-A-G

86928622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671619-G-A

86928837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671403-G-T

86928839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671401-C-T

86929009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671218-A-G

86929028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671200-C-T

86929051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65671176-T-A

http://identifiers.org/hco/3/GRCh38#86929194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65671044-C-A

86929455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670833-G-T

86929586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670698-T-A

86929586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670698-T-C

86929612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670672-G-A

86929645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670627-T-C

86929648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670624-A-G

86929694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670566-G-T

86929990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670302-C-T

86930168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670111-T-G

86930190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670092-C-G

86930209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65670073-A-G

86930797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65669494-T-G

86931098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65669204-T-C

86931565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65669065-A-G

86933565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667964-T-A

86933619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667911-T-C

86933716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667824-G-A

86933857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667673-G-T

86933891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667634-T-A

86934013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667290-C-T

http://identifiers.org/hco/3/GRCh38#86934049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65667239-A-C

86934195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667094-T-C

86934199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667093-C-T

86934316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667018-G-A

86934328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65667006-T-G

86937040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666472-G-A

86937151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666368-G-A

86937151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666368-G-T

86937280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666253-G-C

86937380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666151-T-G

86937464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666073-C-G

86937464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666073-C-T

http://identifiers.org/hco/3/GRCh38#86937465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65666072-C-A

86937465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666072-C-G

86937500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65666037-G-A

http://identifiers.org/hco/3/GRCh38#86937628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65665949-C-A

http://identifiers.org/hco/3/GRCh38#86937981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65665570-A-C

86938033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65665533-G-A

86938168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65665396-T-A

86938168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65665396-T-C

86938216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65665315-T-C

86938249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65665282-T-C

86938774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664752-T-A

86938786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664740-G-A

86938786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664740-G-T

http://identifiers.org/hco/3/GRCh38#86938808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65664717-C-A

86938900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664644-C-T

http://identifiers.org/hco/3/GRCh38#86939044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65664515-C-A

86939072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664477-A-G

86939156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664398-A-G

86939156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664398-A-T

86939611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#86939701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65664188-C-A

86939701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664188-C-T

86939753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664135-G-A

86939796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664097-T-C

86939826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664062-G-A

86939826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65664062-G-T

86940087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65663809-A-T

86940546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65663305-C-T

http://identifiers.org/hco/3/GRCh38#86940596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65663264-C-A

86940596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65663264-C-T

86940847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65663078-T-C

http://identifiers.org/hco/3/GRCh38#86941015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65662895-C-A

86941069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662840-A-T

86941423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662497-A-G

86941423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662497-A-T

86941475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662450-A-G

86941804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662154-A-G

http://identifiers.org/hco/3/GRCh38#86941808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65662150-C-A

86941822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662136-T-C

http://identifiers.org/hco/3/GRCh38#86941913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65662045-C-A

86941913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662045-C-T

86941952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662010-A-G

86941952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65662010-A-T

86941979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661984-C-T

86941980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661983-G-A

86941980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661983-G-C

86942278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661691-A-T

86942471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661495-A-G

86942480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661477-C-T

86942486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661471-T-C

86942498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661459-T-C

http://identifiers.org/hco/3/GRCh38#86942624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65661344-C-A

86942700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661273-T-C

86942700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661273-T-G

86942761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661211-G-A

86942964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65661017-A-G

86943018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660995-T-C

86943032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660981-T-G

86943052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660961-G-A

86943052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660961-G-T

86943056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660957-G-A

86943056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660957-G-T

86943072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660938-T-A

86943072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660938-T-C

86943088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660922-G-A

86943088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660922-G-T

86943138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660880-A-G

86943141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660877-T-A

http://identifiers.org/hco/3/GRCh38#86943253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65660782-C-A

86943288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660751-A-T

http://identifiers.org/hco/3/GRCh38#86943463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65660603-C-A

http://identifiers.org/hco/3/GRCh38#86943518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65660577-A-C

86943518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660577-A-T

http://identifiers.org/hco/3/GRCh38#86943535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65660563-A-C

86943908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660184-A-G

86943908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660184-A-T

86944014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660116-G-T

86944076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: -G-A

86944208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: -G-A

86944246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65660013-T-C

http://identifiers.org/hco/3/GRCh38#86944707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65659756-C-A

86944718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65659747-T-C

86944743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65659722-A-G

86944886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#86945048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65659413-C-A

86945107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65659354-A-G

86945402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65659064-C-T

86945808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658712-A-G

86945817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658703-G-A

86945922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658647-C-T

86945935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658634-A-G

86946021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658569-C-T

86946125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658454-A-G

86946239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658368-G-T

86946313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658299-A-G

86946364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658248-G-A

86946364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65658248-G-T

http://identifiers.org/hco/3/GRCh38#86946486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65658131-A-C

http://identifiers.org/hco/3/GRCh38#86946672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657947-A-C

86946672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657947-A-G

http://identifiers.org/hco/3/GRCh38#86946680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657939-A-C

86946680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657939-A-G

86946680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657939-A-T

http://identifiers.org/hco/3/GRCh38#86946694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657924-C-A

86946694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657924-C-G

86946796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657827-T-A

86946796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657827-T-C

86946817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657806-A-G

86946822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657803-A-G

86946832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657793-A-G

86946886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657736-A-G

86946886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657736-A-T

http://identifiers.org/hco/3/GRCh38#86946887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657735-C-A

86946887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65657735-C-T

http://identifiers.org/hco/3/GRCh38#86947094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657528-A-C

86947094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657528-A-G

86947166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657461-G-C

86947166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657461-G-T

http://identifiers.org/hco/3/GRCh38#86947189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657439-C-A

86947189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657439-C-T

86947250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657409-A-G

http://identifiers.org/hco/3/GRCh38#86947296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65657362-C-A

86947296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657362-C-T

86947323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657333-A-G

86947344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657312-T-C

86947380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657271-G-T

86947490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657166-G-A

86947552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65657103-A-T

86947988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65656693-G-A

86948106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65656585-T-C

86948205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65656289-A-G

86948272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65656227-T-C

86948495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655939-G-A

86948544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655886-T-C

86948809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655732-A-G

86948853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655695-C-T

86948985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655563-T-A

86949108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655441-T-A

86949136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655422-A-G

86949280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65655282-A-G

http://identifiers.org/hco/3/GRCh38#86949516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65655041-C-A

http://identifiers.org/hco/3/GRCh38#86950077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65654844-C-A

86950077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65654844-C-G

86950228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65654699-G-A

http://identifiers.org/hco/3/GRCh38#86950719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65654149-A-C

86951026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65653859-A-T

86951034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65653852-A-G

86951435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65653445-C-G

86951476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65653408-A-G

86951564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65653308-A-G

86951663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65653212-T-C

86951899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652988-G-A

86951919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652975-C-T

86951977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652938-C-T

86952009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652908-T-C

86952112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652811-G-T

86952217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652663-T-C

http://identifiers.org/hco/3/GRCh38#86952322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65652287-A-C

86952490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652128-T-C

86952528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652100-T-G

86952619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65652016-C-G

86952680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651952-C-G

86952773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651865-C-T

86952958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651706-A-G

86953175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651477-A-G

86953365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651288-T-C

86953462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651220-A-T

86953563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651122-T-C

86953564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65651121-G-A

86953623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65649224-G-C

86953684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65649165-G-A

86953740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65649114-T-C

86953828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65649045-T-G

86953894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648979-T-C

86953947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648930-A-G

86954461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648452-C-T

86954555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648394-C-G

86954620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648332-T-A

86954670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648279-A-G

86954784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648173-A-G

86954954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65648007-T-C

86955037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647918-T-A

86955142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647829-C-T

http://identifiers.org/hco/3/GRCh38#86955217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65647770-A-C

86955525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647670-A-T

86955626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647636-G-C

86955757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647565-A-G

86955775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647547-A-T

86956179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647148-T-C

86956294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65647046-G-A

86956347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65646974-T-C

86957072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65646424-G-A

86957116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65646374-G-A

86957355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645971-T-C

86957478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645855-A-G

86957478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645855-A-T

86957498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645837-A-G

86957700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645666-A-T

86957760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645597-G-C

86957844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645487-A-G

86957872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645448-A-G

http://identifiers.org/hco/3/GRCh38#86957946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65645302-A-C

86958065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645185-T-C

86958145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645112-T-C

86958169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65645088-T-G

86958839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65644420-A-T

86959138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65644123-T-C

86959171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65644093-T-A

86959223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65644043-T-C

86959236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65644035-T-C

86959296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643987-T-G

86959321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643963-T-A

86959329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643952-T-A

86959334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643947-A-G

86959335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643946-T-C

86959366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643913-G-C

86959496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643792-C-T

86959507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643781-T-A

http://identifiers.org/hco/3/GRCh38#86959755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65643514-A-C

86959892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643409-T-C

86959920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643376-G-A

http://identifiers.org/hco/3/GRCh38#86959958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65643341-C-A

86960006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643303-C-T

http://identifiers.org/hco/3/GRCh38#86960014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65643295-A-C

86960033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65643278-C-T

86960563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65642107-C-T

86960598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65642072-A-G

86960667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65642011-G-C

86960736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65641950-T-A

86960777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65641916-A-T

86960852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 65641830-G-T

86961164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65641572-T-C

86961196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65641540-G-A

86961529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65641217-G-A

86961788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65640993-A-G

86961880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65640889-C-T

http://identifiers.org/hco/3/GRCh38#86962099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65640678-A-C

86962099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65640678-A-T

86962338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65640510-G-A

86962338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65640510-G-C

86962590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 65640296-T-C

86963310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639967-A-T

86963419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639871-C-G

86963458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639831-A-T

86963517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639763-T-C

86963533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639749-T-C

86963573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639712-T-G

86963586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639699-T-C

86963645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639655-T-C

86963645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639655-T-G

86963791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639552-G-T

http://identifiers.org/hco/3/GRCh38#86963844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65639497-C-A

86964087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639418-C-T

86964328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639275-T-A

86964353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639257-T-A

86964353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639257-T-C

86964437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639186-C-T

86964445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639172-T-C

86964619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639021-A-G

86964619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65639021-A-T

86965236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638748-A-G

86965404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638664-A-G

86965404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638664-A-T

86965528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638589-C-G

86965596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638526-T-C

86965746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638371-T-C

86965773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638346-T-C

86966010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638223-T-C

http://identifiers.org/hco/3/GRCh38#86966050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65638183-A-C

86966116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638128-T-C

86966148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65638094-A-G

http://identifiers.org/hco/3/GRCh38#86966405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65637873-C-A

86966405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637873-C-G

86966405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637873-C-T

http://identifiers.org/hco/3/GRCh38#86966627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65637697-A-C

86966627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637697-A-G

86966635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637689-G-C

86966658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637670-T-C

86966662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637666-A-G

86966708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637636-A-G

86966732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637608-C-T

86966740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637600-T-G

86966752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637588-T-A

86966752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637588-T-C

86966771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637579-G-A

86966784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637566-T-C

86966786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637564-T-C

86966802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637548-T-C

86966824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637526-T-C

86966824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637526-T-G

86967959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65637157-G-A

86968402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65636796-T-G

86968483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65636714-G-T

http://identifiers.org/hco/3/GRCh38#86968545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65636662-A-C

http://identifiers.org/hco/3/GRCh38#86968582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65636625-C-A

86968811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65636405-C-G

86968811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65636405-C-T

86968853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65636363-A-G

86968874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65636342-G-A

86968997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65636219-C-T

86969131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65636085-G-A

86969176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65636045-T-A

86969176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65636045-T-G

86969240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635982-T-C

86969240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635982-T-G

86969252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635970-C-T

86969270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635952-A-G

86969285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635937-G-A

86969285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635937-G-T

86969373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635853-G-A

86969373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635853-G-C

86969378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635848-A-G

86969378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635848-A-T

86969724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635550-C-T

86969815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635457-C-T

86970103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635223-T-A

86970196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635124-A-T

86970206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635114-A-G

86970342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635010-C-G

86970342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65635010-C-T

86970373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634986-G-A

86970373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634986-G-T

86970383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634976-T-A

http://identifiers.org/hco/3/GRCh38#86970440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65634918-C-A

http://identifiers.org/hco/3/GRCh38#86970455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65634896-A-C

86970455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634896-A-G

86970556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634804-T-A

86970556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634804-T-C

86970616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634684-G-A

86970618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634682-G-A

86970688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634619-G-A

86970696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634611-A-G

86970699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634608-T-C

86971014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634292-T-C

86971205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634114-G-A

http://identifiers.org/hco/3/GRCh38#86971262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65634063-C-A

86971262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634063-C-T

86971281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65634043-G-A

86971380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633980-T-C

http://identifiers.org/hco/3/GRCh38#86971528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65633836-A-C

86971928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633662-G-A

86971928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633662-G-C

86972057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633532-G-A

86972224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633366-C-T

86972239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633351-T-G

86972349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633234-G-A

86972502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633074-G-A

86972568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633008-T-C

86972572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65633004-A-T

86972699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65632879-A-T

86972774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65632800-A-T

86972823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65632754-G-A

86972940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65632661-A-T

86973376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65632012-G-C

86973462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65631925-A-G

86973802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, undefined
orthologous variants: 65631590-A-G

http://identifiers.org/hco/3/GRCh38#86973824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65631568-C-A

http://identifiers.org/hco/3/GRCh38#86974143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65631273-A-C

86974144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65631272-G-T

86974447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65631055-G-A

http://identifiers.org/hco/3/GRCh38#86974613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65630879-C-A

http://identifiers.org/hco/3/GRCh38#86975136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65628295-A-C

86975185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65628244-A-T

http://identifiers.org/hco/3/GRCh38#86975308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65628131-C-A

86976265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65627241-T-G

86976353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65627161-C-G

86976353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65627161-C-T

86976527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626990-G-T

86976561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626956-T-C

86976597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626920-T-G

86976683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626836-T-C

86976755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626780-A-T

http://identifiers.org/hco/3/GRCh38#86977009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65626532-A-C

86977057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626490-C-T

86977223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626328-G-A

86977333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626228-C-T

86977488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626085-C-T

86977512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626060-G-T

86977583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65626005-C-T

86977880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625732-A-G

86978070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625539-A-G

86978111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625499-C-T

86978225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625368-G-T

http://identifiers.org/hco/3/GRCh38#86978253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65625340-C-A

86978253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625340-C-T

86978269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625325-C-T

http://identifiers.org/hco/3/GRCh38#86978432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65625153-C-A

86978432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625153-C-G

86978432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65625153-C-T

86978920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65624658-T-C

http://identifiers.org/hco/3/GRCh38#86978922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65624656-C-A

86979256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65624307-G-C

86979256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65624307-G-T

86979524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65624048-T-C

http://identifiers.org/hco/3/GRCh38#86979558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65624014-A-C

86979558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65624014-A-G

http://identifiers.org/hco/3/GRCh38#86979650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65623914-C-A

86979650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623914-C-G

86979668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623896-T-G

86979758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623808-C-G

86980238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623377-T-C

86980251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623365-A-G

86980265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623351-A-G

86980359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623258-A-G

86980417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623205-G-C

86980445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623176-A-T

86980486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623141-T-C

86980568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623047-A-G

86980618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65623014-C-T

86980735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622914-T-G

86980766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622883-A-T

86980840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622814-T-A

86980877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622781-G-A

86980877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622781-G-T

86980888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622770-G-C

86980888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622770-G-T

86980906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622753-T-C

86980911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622748-C-T

86980912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622747-G-A

86981348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622387-A-G

86981382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622349-T-C

86981386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622345-A-G

86981832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65622009-C-T

86982514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65621710-G-A

86982600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65621625-T-C

86982633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65621592-G-T

86982858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65620970-A-T

86983155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65620680-T-C

86983257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65620574-A-G

http://identifiers.org/hco/3/GRCh38#86983269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65620562-A-C

86983934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619717-G-A

86983934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619717-G-C

86983964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619691-G-A

86983971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619684-C-T

86983986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619669-A-G

86984019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619634-C-T

86984281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619257-C-T

86984430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65619095-T-G

86984697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65618828-G-A

86984884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65618648-T-C

86985054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65618484-G-A

86985396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65618138-A-G

86985947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65617582-G-T

86986377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65617229-C-T

86986405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65617202-G-C

86986525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65617084-G-A

86986525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65617084-G-T

86987146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616442-C-T

86987383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616246-A-G

86987413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616216-T-C

86987437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616194-A-G

86987478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616156-C-G

86987478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65616156-C-T

86988065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65615372-A-G

86988119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65615206-A-G

86988249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65615059-C-T

86988282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65615025-T-C

86988589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614715-T-C

http://identifiers.org/hco/3/GRCh38#86988622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65614695-A-C

86988679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614648-A-G

86988679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614648-A-T

http://identifiers.org/hco/3/GRCh38#86988740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65614613-A-C

86988757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614596-T-A

http://identifiers.org/hco/3/GRCh38#86988762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#65614591-C-A

86988762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron_variant, undefined
orthologous variants: 65614591-C-T

86988880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614495-T-C

86988960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614440-T-C

86989165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614225-A-G

86989196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614194-G-A

86989196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614194-G-T

86989204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65614186-C-G

86989525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65613688-A-G

86990055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65613207-C-T

86990115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65613152-C-T

86990249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65613006-T-C

86990382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65612876-G-A

86990382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65612876-G-C

http://identifiers.org/hco/3/GRCh38#86990533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65612726-C-A

86990533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: intron variant
orthologous variants: 65612726-C-T

86990712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: missense variant
orthologous variants: 65612548-T-C

86990803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612457-G-A

86990803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612457-G-T

http://identifiers.org/hco/3/GRCh38#86991043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65612214-C-A

86991043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612214-C-G

86991061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612196-G-A

86991061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612196-G-T

http://identifiers.org/hco/3/GRCh38#86991062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65612195-C-A

86991062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612195-C-T

http://identifiers.org/hco/3/GRCh38#86991106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65612136-C-A

86991106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612136-C-G

86991106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612136-C-T

http://identifiers.org/hco/3/GRCh38#86991128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#65612113-C-A

86991128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24327
most severe consequence: 5 prime UTR variant
orthologous variants: 65612113-C-T