http://identifiers.org/hco/16/GRCh38#21597296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120632072-A-C

21597296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120632072-A-G

21597922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120632648-T-A

21597922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120632648-T-C

21598055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120632717-T-C

21598743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120633080-T-G

21599364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120633654-G-A

21599364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120633654-G-C

21599364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120633654-G-T

21599399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, undefined
orthologous variants: 120633670-A-T

21599410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, undefined
orthologous variants: 120633681-C-T

21599482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, undefined
orthologous variants: 120633746-T-C

21599482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, undefined
orthologous variants: 120633746-T-G

http://identifiers.org/hco/16/GRCh38#21599579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120633845-C-A

21599579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120633845-C-G

21599648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120633941-G-A

21599648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120633941-G-T

21599651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120633944-G-A

21599758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120634058-T-A

21599758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120634058-T-C

21599874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 120634174-G-A

21599874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 120634174-G-C

21599874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 120634174-G-T

21600300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120634569-A-G

21600643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120634900-G-A

21601081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120635305-A-G

21601081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120635305-A-T

21602046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120636663-C-T

http://identifiers.org/hco/16/GRCh38#21603488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120637398-A-C

21604018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120637901-A-G

http://identifiers.org/hco/16/GRCh38#21604520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120638359-C-A

21604520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120638359-C-T

21606722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120640788-C-T

21606960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120641019-A-G

21607064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120641127-A-T

21607443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120641539-T-A

21608224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120641984-C-T

21608804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120642424-T-C

21608876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120642494-T-C

21608979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120642637-A-G

21609871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120643484-T-G

21609886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120643495-A-G

21610008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120643866-A-G

http://identifiers.org/hco/16/GRCh38#21610123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120644003-A-C

21610191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120644067-C-T

21611395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120645541-C-T

21611396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120645542-G-A

21611678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120645791-A-G

21611931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120646273-A-G

http://identifiers.org/hco/16/GRCh38#21611965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120646288-C-A

21611965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120646288-C-T

21612006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120646321-T-A

21612006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120646321-T-C

21612049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120646355-G-A

21612049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120646355-G-T

21612216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120646504-A-G

21612260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120646549-T-C

http://identifiers.org/hco/16/GRCh38#21612302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120646579-C-A

21612610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647035-T-G

21612985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647419-T-A

21612985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647419-T-C

21613057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647489-G-T

21613154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647579-G-C

21613283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647650-A-G

21613373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647775-G-A

21613463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647845-G-A

http://identifiers.org/hco/16/GRCh38#21613595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120647945-C-A

21613639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120647988-T-C

21613844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648176-T-C

21613984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648279-C-T

21614060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648361-G-A

21614063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648364-A-G

21614320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648595-T-G

21614389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120648662-T-C

http://identifiers.org/hco/16/GRCh38#21615169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120649889-A-C

21615201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120649922-A-T

21615621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120650038-A-G

21616251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120650606-G-A

21616251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120650606-G-C

21616462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120650764-A-T

21617810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120651260-T-G

21617831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120651280-A-G

http://identifiers.org/hco/16/GRCh38#21617836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120651288-C-A

21617836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120651288-C-T

21618201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120651724-T-A

21618201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120651724-T-C

21622781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120655005-A-G

21622992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120655184-T-C

21623004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120655196-T-C

21624653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120655805-G-A

21624744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120655870-A-T

21624850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120656024-G-T

21624868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120656042-G-A

21624868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120656042-G-C

21624868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120656042-G-T

21625321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656820-G-A

21625326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656824-A-G

21625346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656844-G-A

21625386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656866-T-G

http://identifiers.org/hco/16/GRCh38#21625397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120656877-A-C

21625463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656932-A-G

21625478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656947-C-G

21625478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120656947-C-T

21626325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120657818-A-G

21626542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120658633-G-A

21626703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120658782-G-A

21626713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120658798-C-T

21627047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659122-A-G

21627066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659139-T-A

21627078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659149-C-G

21627097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659168-T-A

21627123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659194-C-T

21627124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659195-G-A

21627124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659195-G-T

21627160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659238-G-T

21627163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659244-A-G

21627173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659254-T-C

21627267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659301-G-A

21627303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120659334-T-G

21627318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659349-T-C

21627362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659406-T-C

http://identifiers.org/hco/16/GRCh38#21627414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120659461-C-A

21627414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120659461-C-G

21639218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120662719-G-A

21639387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120662840-T-G

21639452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120662894-G-T

21640934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120663809-G-T

http://identifiers.org/hco/16/GRCh38#21641058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120663920-C-A

21641267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664151-G-T

21641299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664201-A-T

21641319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664246-T-C

21641320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664247-G-T

21641394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664321-T-A

21641394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664321-T-C

http://identifiers.org/hco/16/GRCh38#21641400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120664327-C-A

21641400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664327-C-G

21641400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664327-C-T

21641445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664389-T-C

http://identifiers.org/hco/16/GRCh38#21641511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120664662-C-A

21641511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664662-C-T

21641525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664675-A-G

21641525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664675-A-T

21641530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664680-G-A

21641530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120664680-G-T

21641613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120664754-G-C

21641646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120664785-G-A

21641646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120664785-G-T

http://identifiers.org/hco/16/GRCh38#21641661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120664799-A-C

21641661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120664799-A-G

21641891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120665653-T-C

http://identifiers.org/hco/16/GRCh38#21641998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120665742-C-A

http://identifiers.org/hco/16/GRCh38#21642018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120665762-C-A

21642022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120665766-G-T

21642818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666228-C-G

21642933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666304-T-C

21643017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666390-T-G

21643160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120666505-A-G

21643185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666527-C-T

21643492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666755-G-A

21643492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120666755-G-T

21644231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120667444-T-A

21644231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron variant
orthologous variants: 120667444-T-C

21644319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant
orthologous variants: 120667513-C-T

21644367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant
orthologous variants: 120667561-T-C

21644367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant
orthologous variants: 120667561-T-G

21644376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant
orthologous variants: 120667570-C-T

21644486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120667672-G-T

21644489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120667675-G-C

21644489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120667675-G-T

21644491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120667677-G-T

21644843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120668213-G-A

21644894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120668289-A-G

21645000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120668389-T-G

21646309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120669412-T-G

21647122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120669703-C-T

21647422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120670003-G-A

21647422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120670003-G-C

21647422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120670003-G-T

21647490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 120670071-C-T

21647510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120670093-T-A

http://identifiers.org/hco/16/GRCh38#21647874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120670387-C-A

21647874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120670387-C-T

21648716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120670879-G-C

21648926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120671289-G-A

21650756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120671948-A-G

21651587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120672656-C-G

21651648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120672713-C-T

21651684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120672741-T-C

21651729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120672780-T-C

21651927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120672943-A-G

21652104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673264-T-G

21652111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673271-G-A

21652111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673271-G-T

21652362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673501-T-C

21652362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673501-T-G

21652393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673529-G-T

21652401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673537-T-C

http://identifiers.org/hco/16/GRCh38#21652402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120673538-C-A

21652402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673538-C-G

21652402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120673538-C-T

21652892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120673954-A-G

21653059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120674113-A-G

21654431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120674787-G-A

21654431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120674787-G-T

21654462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120674814-C-T

21654541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120674886-A-G

21654803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675026-A-G

21654844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675063-T-C

21654847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675066-T-C

21654889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675100-A-G

21654952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675134-A-G

21655059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675206-A-G

http://identifiers.org/hco/16/GRCh38#21655095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120675241-C-A

21655095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675241-C-T

21655164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120675291-T-C

21655405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120675531-C-T

21655406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120675532-G-A

21655445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675571-C-T

http://identifiers.org/hco/16/GRCh38#21655465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120675588-C-A

21655473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675596-G-A

21655476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675599-G-A

21655476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675599-G-T

http://identifiers.org/hco/16/GRCh38#21655494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120675617-C-A

21655502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675623-A-G

21655502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675623-A-T

21655611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675730-T-A

21655611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675730-T-C

21655611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675730-T-G

21655618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675735-C-T

21655659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675777-C-T

21655666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675784-A-G

21655667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675785-C-T

http://identifiers.org/hco/16/GRCh38#21655697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120675815-A-C

21655774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675892-A-G

http://identifiers.org/hco/16/GRCh38#21655777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120675895-C-A

21655870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120675993-A-G

21655970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676077-C-T

21655999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676104-G-A

21656053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676156-G-A

21656053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676156-G-T

http://identifiers.org/hco/16/GRCh38#21656105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120676198-A-C

21656105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676198-A-G

http://identifiers.org/hco/16/GRCh38#21656142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120676218-C-A

21656142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676218-C-T

21656153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676229-T-C

21656650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676629-G-A

21656860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120676764-A-G

21656925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676828-G-T

http://identifiers.org/hco/16/GRCh38#21657029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120676918-C-A

21657029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120676918-C-T

21657129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120677000-T-C

http://identifiers.org/hco/16/GRCh38#21657377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120677216-C-A

21657399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120677238-A-G

21657401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120677240-G-A

21657401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120677240-G-T

21657404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120677243-T-C

21657418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24586
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120677252-A-G