186429555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150228097-C-T

186434132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150225063-A-G

186434142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150225053-G-A

186434614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150224580-G-A

186434735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150223904-C-T

186434740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150223899-A-G

186434965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150223678-G-A

186434980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150223663-T-C

186435066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150223562-A-G

186435134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150223494-A-G

186435135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150223493-A-G

http://identifiers.org/hco/1/GRCh38#186435196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150223429-C-A

186435227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 150223400-T-C

186435246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150223381-T-C

186435253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150223374-G-T

186435256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150223371-G-A

186435758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150222163-A-G

186436085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150221871-T-A

186436109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150221845-A-G

186436157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150220909-T-C

http://identifiers.org/hco/1/GRCh38#186436206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220864-C-A

http://identifiers.org/hco/1/GRCh38#186436255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220819-C-A

http://identifiers.org/hco/1/GRCh38#186436322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220753-C-A

186436343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220732-T-A

186436343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220732-T-C

186436353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150220722-C-T

186436354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150220721-G-A

186436354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150220721-G-T

186436377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150220698-A-G

186436378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150220697-G-T

186436384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150220691-T-C

http://identifiers.org/hco/1/GRCh38#186436392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220683-C-A

186436392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150220683-C-T

186436412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: 150220663-A-G

http://identifiers.org/hco/1/GRCh38#186436456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220619-C-A

186436695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220379-A-G

http://identifiers.org/hco/1/GRCh38#186436710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150220364-C-A

186436815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220285-G-A

186436868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220233-A-G

186436935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150220199-T-A

186439844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213551-A-G

186439981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213416-C-T

186440048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213350-G-C

186440253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213135-A-G

186440273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213123-A-G

186440273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150213123-A-T

186440508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212896-G-A

186440563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212841-G-A

186440757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212564-G-A

186441117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212166-C-G

186441117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212166-C-T

186441224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150212069-A-T

186441499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211665-T-C

186441499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211665-T-G

186441749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211409-C-T

186441810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211361-G-T

186441872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211316-G-A

186442204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211095-T-A

186442291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211062-G-A

186442314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150211039-A-T

186442384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150210958-T-A

186442384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150210958-T-C

186442574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150210775-A-T

http://identifiers.org/hco/1/GRCh38#186442576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150210773-A-C

186442644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150210706-G-A

186443141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150210106-T-C

186443683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209556-G-C

186443697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209541-A-G

http://identifiers.org/hco/1/GRCh38#186443776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150209460-C-A

186443776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209460-C-T

186443872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209365-T-G

http://identifiers.org/hco/1/GRCh38#186443878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150209359-A-C

186443878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209359-A-G

http://identifiers.org/hco/1/GRCh38#186443935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150209295-C-A

http://identifiers.org/hco/1/GRCh38#186443968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150209262-A-C

186443968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209262-A-G

186443968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209262-A-T

186444105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209125-A-G

186444145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150209085-T-C

186444238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150208992-T-C

186444285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150208945-A-G

186444369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150208861-C-T

186444433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150208797-T-C

186444538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208685-G-A

186444538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208685-G-T

http://identifiers.org/hco/1/GRCh38#186444541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150208682-A-C

186444573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208651-T-C

186444573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208651-T-G

186444585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208639-G-A

186444585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208639-G-T

186444605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208614-T-G

186444622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208597-C-G

186444624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208595-T-A

186444624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208595-T-C

186444712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208536-G-A

186444970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208363-G-A

186445006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208327-G-A

186445192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208188-G-A

186445192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208188-G-C

186445437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208022-C-G

186445437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150208022-C-T

http://identifiers.org/hco/1/GRCh38#186446197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150206815-A-C

186446236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206776-T-C

186446293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206726-T-C

186446401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206644-A-G

186446490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150206562-A-G

186446612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206444-T-A

186446612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206444-T-C

186447772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150206025-T-C

186448125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205804-A-G

186448178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205764-T-A

186448178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205764-T-C

186448186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205756-G-T

186448190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205752-A-G

186448259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205679-G-A

186448456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205114-C-G

186448535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205033-G-T

186448545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205023-T-A

186448545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150205023-T-C

186448691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204859-A-G

186448692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204858-C-T

186448709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204841-A-G

186448714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204836-T-C

186448864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204669-T-A

186448949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204587-A-T

186449014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204536-G-T

186449089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204472-T-C

http://identifiers.org/hco/1/GRCh38#186449254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150204289-C-A

186449254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204289-C-G

186449254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204289-C-T

186449268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204275-T-C

186449355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204193-T-C

186449370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204178-T-A

186449370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204178-T-C

186449370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204178-T-G

http://identifiers.org/hco/1/GRCh38#186449385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150204163-C-A

186449385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204163-C-T

186449428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204120-T-C

186449428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150204120-T-G

186449499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204050-A-G

186449535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150204015-T-C

186449579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203971-G-T

186449586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203964-G-A

186449586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203964-G-C

186449586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203964-G-T

186449593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203957-G-A

186449593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203957-G-T

186449610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203945-A-G

186449741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203831-T-C

186449772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203796-A-G

186449916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203086-T-C

186449918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203084-T-C

186449921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203081-G-A

186449964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150203040-A-G

http://identifiers.org/hco/1/GRCh38#186450955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150202431-C-A

186450955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150202431-C-T

186450992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150202393-C-T

186451043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150202344-G-T

186451481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150201826-G-T

186451482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150201825-A-G

186451640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150201660-T-A

186451816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150201558-A-T

186452110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150201303-T-C

186452129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150201285-T-C

186452777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150200216-G-A

186452777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150200216-G-T

186457008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150198284-G-A

186457062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150198230-A-G

186457165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150198130-A-G

186457301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150198006-G-T

186457623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150196924-G-T

186458159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150196424-C-T

186458225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150196361-T-C

186459685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150196112-A-G

186459799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150196028-G-T

186459867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150195954-A-T

186459891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150195930-A-G

186460141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150195691-C-T

186460712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150195586-G-C

186460848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150195441-A-T

186461081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150195215-G-A

186461091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150195199-A-G

186461093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150195197-T-C

http://identifiers.org/hco/1/GRCh38#186461118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150195172-C-A

186461648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150193225-G-T

186461751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150193126-A-G

186461940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150192935-A-G

186462433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150192538-T-C

186477543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190696-T-G

http://identifiers.org/hco/1/GRCh38#186477736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150190489-C-A

186477736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190489-C-T

186477765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190456-A-G

http://identifiers.org/hco/1/GRCh38#186477924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150190290-C-A

186477986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190236-G-A

186477995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190227-A-T

186478017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190205-G-A

186478077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190161-A-G

186478103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190135-G-A

186478183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150190061-G-T

186478376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189829-A-G

186478403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189804-A-G

186478539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189477-T-C

186478774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189283-G-T

186478945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189119-C-T

186478952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150189113-A-G

186479151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188920-C-T

186479240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188839-G-A

186479267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188812-T-C

186479522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188567-C-T

186479539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188550-A-G

186479644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150188452-G-T

186480208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187381-T-C

http://identifiers.org/hco/1/GRCh38#186480212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150187377-A-C

186480449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187164-G-C

186480449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150187164-G-T

186480694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186993-G-A

186480790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186895-G-T

186480832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186867-A-G

186481217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150186406-G-C

http://identifiers.org/hco/1/GRCh38#186481465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150186007-C-A

186481656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150185814-G-A

http://identifiers.org/hco/1/GRCh38#186482750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150183670-A-C

186482756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183664-C-T

186482771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183648-G-A

186482786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183633-G-A

http://identifiers.org/hco/1/GRCh38#186482850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150183574-C-A

186482850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183574-C-G

186482850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183574-C-T

186482873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150183551-A-T

186483165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183110-A-G

186483188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183087-G-A

186483202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183073-A-G

186483261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150183015-G-A

186483274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182998-T-C

186483313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150182965-A-G

186484497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150139873-G-C

186484616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150139755-A-G

186484643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150139728-C-T

186484653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150139718-G-A

186484771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150139593-G-A

http://identifiers.org/hco/1/GRCh38#186484894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150139470-A-C

186485122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150138126-T-C

186485130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150138118-A-G

186485130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150138118-A-T

186485151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150138098-C-G

186485151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150138098-C-T

186485260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137990-G-A

186485347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137930-A-T

186485678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137697-G-A

186485967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137430-A-G

186486074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137325-T-G

186486279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150137130-C-T

186486583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136825-A-G

186486631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136772-G-A

186486650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136753-C-T

186486686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136720-G-T

186486779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136639-C-T

186486967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136451-T-C

186486974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136444-C-T

186487020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136397-T-C

186487075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136342-T-C

186487090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150136333-G-T

186487696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135801-A-G

186487956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135561-A-G

186488425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135195-C-T

186488503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135122-A-T

186488585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135044-C-T

186488593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150135036-A-G

186488652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150134978-G-A

186488660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150134970-G-A

186488744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150134906-A-T

186489488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150133331-A-T

186489597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150133209-T-G

186490330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150132574-G-A

186490601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150132066-C-T

http://identifiers.org/hco/1/GRCh38#186490663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150132005-C-A

186490663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150132005-C-T

186492471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130910-C-T

186492720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130662-T-C

186493008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130373-C-G

186493026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130356-A-G

186493026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130356-A-T

http://identifiers.org/hco/1/GRCh38#186493073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150130306-A-C

186493309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150130037-A-G

186494741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127816-G-A

186494862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127701-G-A

186494968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127625-C-G

186494974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150127619-G-A

186495002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127588-T-C

186495013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127577-G-A

186495408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150127155-C-G

186495796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150126631-G-A

186496000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150126398-G-C

186496146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150126256-A-G

186496485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125567-C-T

186496746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125293-A-T

186496808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125250-G-A

186496808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125250-G-T

http://identifiers.org/hco/1/GRCh38#186496809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150125249-A-C

186496809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125249-A-G

186496809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125249-A-T

http://identifiers.org/hco/1/GRCh38#186496816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150125242-C-A

186496816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150125242-C-T

186497644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124851-A-T

186497649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124846-A-T

186498401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124468-A-G

186498514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124401-C-T

http://identifiers.org/hco/1/GRCh38#186498809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150124162-C-A

186498841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124132-T-C

186498856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124117-G-A

186498886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124091-T-A

186498886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150124091-T-C

186499258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40432
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150123679-C-G