168249887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29136945-A-G

168249891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29136949-C-T

http://identifiers.org/hco/3/GRCh38#168249895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#29136953-C-A

168249895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29136953-C-T

http://identifiers.org/hco/3/GRCh38#168249898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#29136956-C-A

168249899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29136957-G-A

168249901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29136959-G-A

168249995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29137055-G-A

168249995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29137055-G-T

168250056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29137116-C-T

http://identifiers.org/hco/3/GRCh38#168250084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29137148-C-A

168250084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137148-C-G

168250084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137148-C-T

http://identifiers.org/hco/3/GRCh38#168250098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29137165-C-A

168250098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137165-C-G

168250098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137165-C-T

168250118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29137185-C-T

168250153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137223-G-T

http://identifiers.org/hco/3/GRCh38#168250165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29137238-C-A

168250165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137238-C-T

168250166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137239-G-A

168250191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29137269-A-G

168250220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137297-C-T

168250224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137301-G-C

168250270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29137344-C-T

168250321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29137404-C-T

168250441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137511-G-T

168250763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137760-T-G

168250935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137918-G-T

168251220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29138185-A-G

168251381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29138332-G-A

168251381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29138332-G-C

168251658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29138549-T-A

168251658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29138549-T-C

168252216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139088-G-A

168252344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139227-G-C

http://identifiers.org/hco/3/GRCh38#168252350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29139233-C-A

168252577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139439-A-G

168252814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139931-G-T

168252833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139949-G-A

168252860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29139964-G-C

168253047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140161-G-A

168253127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140241-A-G

168253160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140275-A-G

168257693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150824-A-G

168257732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150877-A-G

168257733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150878-T-G

168257755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150896-T-C

168257847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151027-C-T

168257899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151087-G-A

168257899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151087-G-C

168257929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151117-C-T

168257933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151121-C-G

168257978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151162-A-G

168258143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151293-G-C

168258149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151299-A-G

168258315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151459-C-T

168258386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151529-G-C

http://identifiers.org/hco/3/GRCh38#168258419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29151561-A-C

168258456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151600-G-A

168258682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29153217-G-A

http://identifiers.org/hco/3/GRCh38#168258848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29153360-C-A

168258848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29153360-C-G

168258999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29153501-A-G

http://identifiers.org/hco/3/GRCh38#168259039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29153537-C-A

168259064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29153561-G-A

168259291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29153746-T-C

168260232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29154686-G-A

168260263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29154710-G-A

168260356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29154806-G-T

168260809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155342-G-A

168260995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155509-G-C

168261103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155607-G-A

http://identifiers.org/hco/3/GRCh38#168261133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29155637-C-A

168261288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155757-G-A

168261413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155866-G-A

168261638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156096-T-C

168261660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156119-C-G

http://identifiers.org/hco/3/GRCh38#168261675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29156135-C-A

http://identifiers.org/hco/3/GRCh38#168261692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29156152-C-A

168261715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156175-C-G

168261715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156175-C-T

168261808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156275-G-A

168261875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156386-G-C

168261982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156490-C-T

168262115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156624-T-G

168262567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157095-T-C

168262767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157289-T-C

168262767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157289-T-G

168262799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157322-T-C

168262826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157349-G-A

http://identifiers.org/hco/3/GRCh38#168262931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29157434-A-C

168263622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158477-T-C

168263636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158491-A-G

168264058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159717-C-T

168264324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159960-A-T

168265864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163587-C-G

168265942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163666-C-T

168266195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163884-T-C

168266727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29164364-A-G

168266771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29164408-A-G

168268710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165021-G-A

168268736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165034-T-G

168268806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165091-C-G

168268868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165149-A-G

168268890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165171-T-C

168268911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165184-G-A

168269084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165351-A-G

168269094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165361-A-G

168269121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165388-G-A

168269121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165388-G-C

168269134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165400-T-C

168269178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165437-A-G

168269298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165543-T-G

168269397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165642-A-G

168269646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165890-G-A

168270003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29166320-C-T

168270116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29166439-G-T

168271369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167595-A-G

168271380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167606-A-G

168271432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167655-A-G

168271581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167806-C-T

http://identifiers.org/hco/3/GRCh38#168271587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29167812-A-C

168271635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167850-T-C

168271676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167889-A-G

168271790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168021-T-G

168271919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168145-A-G

168271919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168145-A-T

168271972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168195-G-A

168271976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168199-A-T

168272438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29168695-G-C

168272457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168717-A-G

168272473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168733-T-C

168272757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169011-A-G

168272813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169080-G-A

168272813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169080-G-C

168273095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169516-G-T

168273255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169817-A-G

168273290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169851-G-A

168273498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170034-T-G

168273726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170247-C-T

168273879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170387-G-C

168273987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170490-A-G

168274187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170614-C-G

168274261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170683-C-G

168274261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170683-C-T

168274302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170717-G-A

168274404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170812-T-A

168274513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170900-A-G

168274513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170900-A-T

168274537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170927-C-T

168274542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170972-G-A

168274627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171057-T-C

168274691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171100-G-T

168274844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171200-G-A

168274927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171280-G-A

168275515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172226-A-G

168275685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172309-G-A

168275685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172309-G-T

168275867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172490-C-G

168275867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172490-C-T

168275958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172576-G-A

168277385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29173986-A-G

168277504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29174101-C-T

http://identifiers.org/hco/3/GRCh38#168277597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29174185-C-A

168277875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175184-T-G

168277992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175296-G-A

168277996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175300-A-G

168278052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175353-A-G

168278084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175370-G-A

168278103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175388-G-A

168278246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175518-C-T

168278341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175609-G-T

168278387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175656-G-A

168278484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175765-G-A

http://identifiers.org/hco/3/GRCh38#168278627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29175897-A-C

168278759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176419-T-C

168278831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176492-A-G

http://identifiers.org/hco/3/GRCh38#168278875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29176535-A-C

168279657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29177300-T-C

168279657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29177300-T-G

http://identifiers.org/hco/3/GRCh38#168280145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29177776-C-A

168280788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179233-A-G

168280922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179366-C-G

168281191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179626-T-C

168281248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179680-C-T

168281276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179722-A-G

168281371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29179814-C-T

168282143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180691-A-G

168282148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180696-C-G

168282151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180699-G-T

168282277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180781-T-C

168283005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29182014-A-G

168285950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186055-T-A

168285950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186055-T-G

168286058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186240-G-A

168286393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186577-A-G

168286425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186605-A-G

168286505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186686-G-A

168286698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29186872-T-A

http://identifiers.org/hco/3/GRCh38#168287002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29187186-A-C

168287002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29187186-A-G

168287026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29187209-G-T

168287093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29187286-A-G

168287147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29187344-G-A

168287723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188884-A-G

168287782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188938-C-T

168287825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188979-C-T

168287839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188993-C-T

168287840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188994-A-G

168287927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189081-A-G

168287939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189093-G-A

168288026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189184-C-T

168288093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189241-T-A

http://identifiers.org/hco/3/GRCh38#168288100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29189248-A-C

168288117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189265-A-G

http://identifiers.org/hco/3/GRCh38#168288141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29189288-A-C

168288198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189389-C-T

168288231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189425-C-T

http://identifiers.org/hco/3/GRCh38#168288674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29189869-C-A

168288777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29189958-C-T

http://identifiers.org/hco/3/GRCh38#168288987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29190164-C-A

168289798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190977-A-G

168289940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29191157-A-G

168290007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29191225-C-T

168291268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192241-G-T

http://identifiers.org/hco/3/GRCh38#168291305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29192282-C-A

168291334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192311-A-G

168291411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192388-G-A

168291598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192549-G-A

168291815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192807-A-T

168291893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192882-T-G

168292279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29193264-T-C

168292333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29193330-C-T

http://identifiers.org/hco/3/GRCh38#168292411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29193414-A-C

168292478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29193477-T-C

168298065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195732-G-T

168298157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195820-C-T

http://identifiers.org/hco/3/GRCh38#168298290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29195921-A-C

168298431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196054-G-C

168298679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196235-A-G

168298738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196256-G-A

168299059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196458-G-A

168299203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196567-T-C

168299440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196755-G-A

168299440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196755-G-C

168299600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196911-G-A

168300626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29197956-A-G

168300759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198081-A-G

168300770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198092-T-G

http://identifiers.org/hco/3/GRCh38#168300889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29198185-A-C

168300934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198227-T-A

168301008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198301-G-A

168301202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198504-A-G

168301692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198659-C-T

http://identifiers.org/hco/3/GRCh38#168301746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29198713-A-C

168301916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198959-A-G

168301931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29198978-T-G

168302056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29199096-A-G

168302067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29199107-T-C

168302072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29199112-C-G

168307676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29199486-C-T

168307690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29199500-G-A

168308616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201424-C-T

168308646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201453-A-G

168308716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201543-A-T

168308870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201743-C-T

168308904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201782-G-C

168309080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201944-T-A

168309080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201944-T-C

168309107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201967-A-T

168309216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29202351-G-A

168309216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29202351-G-T

168309522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29202735-T-G

168309541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29202754-G-A

168309541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29202754-G-T

168309878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203092-G-A

168310248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203447-G-A

168310248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203447-G-C

168310248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203447-G-T

168310950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204547-T-G

168311078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204683-A-G

168311431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205010-G-A

168311542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205112-G-A

http://identifiers.org/hco/3/GRCh38#168311710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29205502-C-A

168311871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205654-T-G

168311939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205722-A-G

168311949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205732-A-G

168312079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29205845-G-A

168312371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206119-T-C

168312516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206469-A-G

168312589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206539-C-G

168312603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206552-G-A

168312758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206706-G-A

168312855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29206801-C-T

168313130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207067-G-A

168313861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207421-C-G

168313871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207433-A-G

168313871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207433-A-T

168313970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207538-T-A

168313995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207563-A-G

168314013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207593-G-T

168314027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207607-C-G

168314027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207607-C-T

168314125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29207700-G-A

168314359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29207902-T-C

http://identifiers.org/hco/3/GRCh38#168315553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29208858-A-C

168315553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29208858-A-G

168315874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209172-G-A

168316006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209300-A-G

168316131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209401-T-A

168316226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209492-G-A

168316557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209628-A-G

168316689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209753-A-G

168317276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209954-C-T

168317315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29209996-G-C

http://identifiers.org/hco/3/GRCh38#168317432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29210097-C-A

168317500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29210165-A-G

http://identifiers.org/hco/3/GRCh38#168317773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29210447-A-C

168317858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29210491-A-T

168318244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29210604-T-C

168318991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29210962-G-T

168319624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211548-C-T

168319703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211625-T-C

168319705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211627-A-G

168319810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211732-C-T

168319955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211885-T-G

168320004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29211937-A-G

168320123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212051-G-A

168320486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212365-A-G

168320571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212441-C-T

168320592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212462-G-C

168320646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212519-T-C

168321011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29212959-C-T

168321976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29213031-G-A

168322100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29213170-T-A

168322198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29213265-C-T

168322436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29213489-T-C

168322811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29213947-T-G

168323008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29214258-G-A

168323323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29214570-C-T

168324482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29215135-T-C

168324947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29215531-T-C

168325443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29216055-C-T

168325799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29216556-C-T

http://identifiers.org/hco/3/GRCh38#168325967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29216727-A-C

http://identifiers.org/hco/3/GRCh38#168326199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29217702-A-C

168326199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217702-A-G

168326247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217748-T-A

168326774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29218271-A-G

168326832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29218334-A-T

168326922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29218419-A-G

168327053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29218552-A-G

168327703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219170-T-A

168327775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219241-C-T

http://identifiers.org/hco/3/GRCh38#168327861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29219324-C-A

168327898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219361-A-G

168328068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219523-G-C

168328175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219775-T-C

168328202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29219864-G-C

168328316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220061-C-G

168328521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220256-T-C

168328753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220440-G-A

168328962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220648-T-A

168328968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220654-G-A

168329048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220730-T-C

168329107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220785-T-C

168329349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29220954-A-G

168329662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29221749-T-A

168329966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29222015-G-A

168330033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29222510-T-G

168330172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29222645-C-T

168330175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29222648-G-T

168330504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29222972-G-T

http://identifiers.org/hco/3/GRCh38#168331168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#29223615-C-A

168331168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29223615-C-T

168331169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29223616-G-A

168331420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29223843-T-A

168331659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29224058-T-G

168331836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29224254-C-T

168332105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29224501-T-C

168332295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29224822-A-G

168332759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29225258-C-T

168332776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29225275-T-C

168333025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29225523-T-C

168333122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29225617-G-A

168333306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29225801-T-A

168334024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29226536-G-A

168335510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29230328-G-A

168335677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29230563-A-G

168335751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29230638-A-G

168335955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29230868-G-A

168336185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29231080-G-C

168336386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29231204-G-T

168336584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29231388-C-T

168336815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29231631-G-A

168336821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29231637-A-G

168337304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232070-T-G

168337333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232099-C-G

168337364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232130-G-A

168337613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232332-C-T

168337713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232416-G-A

168337797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232519-C-G

168337862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232775-A-G

168338039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29232955-C-T

168338110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233060-G-A

http://identifiers.org/hco/3/GRCh38#168338195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29233154-C-A

168338195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233154-C-T

168338225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233184-A-G

168338267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233213-C-T

168338272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233219-A-G

168338276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233223-G-A

168338276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233223-G-T

168338757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233690-T-A

168338800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233725-C-T

168338854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233770-A-G

168339264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233828-G-A

168339264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233828-G-T

168339301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233879-G-C

168339434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29233963-A-G

168341071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235760-G-C

168341079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235765-A-G

168341149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235829-G-A

168341165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235860-C-G

168341281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235998-A-G

168341281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29235998-A-T

168341336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29236053-A-G

168341351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29236069-T-C

168341632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29236343-A-G

168341740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29236449-A-G

168341915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29236588-G-A

168341933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29236605-A-G

168342438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237112-C-T

168343095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237781-G-A

168343189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237845-C-T

168343192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237848-C-T

168343197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29237853-T-C

168343744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238319-C-T

168344146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238724-G-T

168344185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29238763-G-A

168344527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239103-C-T

168345132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239676-T-C

168345182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239714-T-C

168345189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239721-G-T

168345199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239730-C-T

168345220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29239751-G-T

168345484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240205-T-A

168345850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240565-C-T

168346299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29240981-T-C

http://identifiers.org/hco/3/GRCh38#168346488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29241115-C-A

168346792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241214-G-T

168346944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241355-A-G

168346954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241365-A-T

http://identifiers.org/hco/3/GRCh38#168347115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29241512-A-C

168347208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29241601-C-T

http://identifiers.org/hco/3/GRCh38#168347326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29242698-C-A

168347456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29242816-C-T

http://identifiers.org/hco/3/GRCh38#168347552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29242917-C-A

168347860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243434-G-A

168347916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243489-G-C

168348025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243598-A-G

168348025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29243598-A-T

168357069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29244394-C-T

168357272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29244585-A-T

168357604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29245043-A-G

168357755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247447-G-C

168357792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247482-A-G

168357793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247483-T-C

168357849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247543-G-T

168357883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247577-T-G

168358192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29247866-A-G

168358449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248117-C-T

168358527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248212-G-A

168358527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248212-G-T

168358683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248420-A-G

168358767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248495-C-G

168358898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248610-C-G

http://identifiers.org/hco/3/GRCh38#168358923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29248634-C-A

168358946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248648-T-G

168359075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248768-G-A

http://identifiers.org/hco/3/GRCh38#168359135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29248826-A-C

168359135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248826-A-G

168359162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248841-T-C

168359251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29248923-G-T

168359709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249396-C-T

168359904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249575-T-C

http://identifiers.org/hco/3/GRCh38#168360121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29249808-C-A

168360121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249808-C-G

168360121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249808-C-T

168360226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249898-C-T

168360248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29249920-A-G

168360778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29250456-C-T

168360997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29250691-C-T

168361542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251178-T-C

168361809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251430-A-G

168361966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29251703-T-C

168362637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252552-C-G

168362667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252582-C-T

http://identifiers.org/hco/3/GRCh38#168363024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29252938-C-A

168363024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29252938-C-T

168363222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29253127-A-G

168363560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29253461-C-T

168363738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29253648-G-C

168364038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29253988-A-G

168364178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254138-T-C

168364182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254142-A-G

168364187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254147-A-G

168364927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254724-C-T

168365044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254885-A-T

168365045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254886-T-C

168365092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254933-G-A

168365130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29254971-A-T

168365371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255212-T-C

http://identifiers.org/hco/3/GRCh38#168365420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29255262-A-C

168365460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255305-T-C

168365471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255316-A-T

168365793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255700-T-C

168365951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29255841-A-G

http://identifiers.org/hco/3/GRCh38#168366070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29256790-A-C

168366132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29256839-T-C

168366186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29256875-G-A

http://identifiers.org/hco/3/GRCh38#168366258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29256934-A-C

168366610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257265-A-T

168366619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257274-A-G

168366656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257434-A-G

168366692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257514-T-G

168366761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257584-A-G

168366873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257690-C-T

http://identifiers.org/hco/3/GRCh38#168366910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29257728-A-C

168366926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29257744-G-A

168367442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29260057-A-T

168367534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29260132-T-C

168367600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29260174-T-C

http://identifiers.org/hco/3/GRCh38#168367744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29260276-A-C

168367751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29260283-T-G

168369307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29262081-C-T

168369309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29262083-A-G

168372211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265253-G-C

168372539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265579-G-T

168372559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265599-T-C

168372782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265842-T-C

168372839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29265899-G-T

168373002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266039-C-T

168373423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266163-A-G

168373434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266174-C-G

http://identifiers.org/hco/3/GRCh38#168373469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29266207-C-A

168373506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266245-T-G

168373818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266543-C-G

168373849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266573-G-A

168373887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266611-A-G

168373887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266611-A-T

168374040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29266973-A-G

168374146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267089-G-A

168374146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267089-G-C

168374172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267115-T-C

168374740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267721-T-A

168374773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267752-A-G

168374857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29267831-T-C

168375527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268470-A-G

168375539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268482-A-G

168375561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268504-T-C

http://identifiers.org/hco/3/GRCh38#168375608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29268559-A-C

168375636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29268586-A-G

168376165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269085-T-G

http://identifiers.org/hco/3/GRCh38#168376615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29269484-C-A

168376659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269530-G-A

168377023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29269855-T-C

168395349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282106-G-A

168395452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282213-G-T

168396148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282787-T-C

168396329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282971-G-A

168396329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282971-G-C

168396333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282975-G-C

168396354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282995-G-A

168396354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29282995-G-C

168396375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29283020-C-T

168396509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29283135-G-A

168396509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29283135-G-T

168396614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29283256-A-T

http://identifiers.org/hco/3/GRCh38#168396849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29283493-C-A

168397449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284086-T-C

168397478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284113-G-T

168397507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284142-G-A

168397562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284196-T-C

168397656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284423-G-A

168397731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284488-A-G

168397862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284613-A-G

168397867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29284618-A-G

http://identifiers.org/hco/3/GRCh38#168398006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29285220-C-A

168398219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29285494-C-T

168398361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286209-C-T

168398403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286232-T-C

168398594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29286420-A-G

http://identifiers.org/hco/3/GRCh38#168398605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29286431-C-A

168399193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29287022-A-G

168399337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29287144-T-G

168399753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29287566-T-C

168399831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29287641-C-T

168399851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29287661-A-G

168400495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289255-G-A

http://identifiers.org/hco/3/GRCh38#168400542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29289304-C-A

168400542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289304-C-T

168400546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289308-G-A

168400564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289324-G-A

168400564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289324-G-T

168400601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29289360-G-T

168401345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29290112-A-G

168401730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29290430-T-C

http://identifiers.org/hco/3/GRCh38#168401740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29290440-C-A

168401740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29290440-C-T

http://identifiers.org/hco/3/GRCh38#168402450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29290860-C-A

168402476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29290886-A-G

http://identifiers.org/hco/3/GRCh38#168402701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29291084-A-C

168402963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29291251-G-A

168403866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29291432-A-G

168404054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29291573-C-T

168404087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29291598-A-G

http://identifiers.org/hco/3/GRCh38#168404173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29291662-A-C

http://identifiers.org/hco/3/GRCh38#168404184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29291673-C-A

http://identifiers.org/hco/3/GRCh38#168404402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

168404865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293228-G-T

168404941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293304-G-A

168404941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293304-G-C

168404941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293304-G-T

168405003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293366-A-T

168405040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293407-A-G

168405086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293449-G-A

http://identifiers.org/hco/3/GRCh38#168405105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29293467-A-C

168405209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293569-T-C

168405209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293569-T-G

168405401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293770-C-T

168405416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293786-G-A

168405417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293787-C-T

168405456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293826-C-G

168405456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29293826-C-T

168405703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294080-A-G

168405716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294096-A-G

168405742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294125-T-C

168405743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294126-G-A

http://identifiers.org/hco/3/GRCh38#168405975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29294339-C-A

168405993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294365-A-G

168406004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294376-T-C

168406004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294376-T-G

168406045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294883-T-C

168406125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294963-A-G

168406125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294963-A-T

168406314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295147-A-G

168406365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295194-A-T

168406493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295323-A-G

168406548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295378-C-T

168406589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295430-A-G

168406928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29296292-T-G

168409355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297070-A-G

168409407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297125-A-G

168409682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297332-T-C

168409873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297518-T-G

168410187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297839-G-A

168410313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29297967-C-T

http://identifiers.org/hco/3/GRCh38#168410623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29298255-A-C

168413847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316606-A-G

168413918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316670-T-G

168413949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316694-G-T

168413966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316711-C-T

168414019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316764-A-G

168415047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317347-A-G

168415047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317347-A-T

168415058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317356-G-T

168415118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317414-G-T

168415155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317450-T-C

168415188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317482-G-C

168415194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317488-G-C

168415223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29317516-T-C

168415683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318043-C-T

168416081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318455-T-C

168416107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318484-C-T

168416141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318517-C-T

168416157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318533-T-C

http://identifiers.org/hco/3/GRCh38#168416179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29318554-A-C

168416179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318554-A-G

168416360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29318720-G-A

168416867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29319610-G-T

168417020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29319769-C-G

168417063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29319811-T-G

168417118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29319909-A-G

168417163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29319954-A-G

168417579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29320408-T-C

168417811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29320639-T-A

168417987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29320796-G-A

168418093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29320855-G-A

168418093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29320855-G-T

168418382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321098-T-C

168418465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321178-T-C

168418465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321178-T-G

168418521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321234-T-C

168418553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321268-A-G

168418584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321299-C-T

168418610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321324-C-G

168418610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321324-C-T

168418822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321534-C-T

168418824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321536-G-C

168418824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321536-G-T

168418853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321570-T-C

168418864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321581-C-T

168418881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321624-C-T

168419160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321805-G-A

168419160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321805-G-T

168419258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321906-T-A

168419258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321906-T-C

168419448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29322049-A-T

168421660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29326476-A-T

168421742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29326543-A-T

http://identifiers.org/hco/3/GRCh38#168422335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29327064-C-A

168422425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327154-A-G

168422437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327166-T-A

168422437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327166-T-C

168422933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327704-G-A

168422971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327758-T-G

168423123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327920-G-C

168423858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329588-A-G

168423870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329600-T-A

168424030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329713-T-A

168424061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329744-A-G

168424078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329760-A-G

168424166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329857-A-G

168424298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29329993-G-A

168424585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29330275-G-A

168424830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331043-C-T

168424985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331176-A-G

168425427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331541-A-G

168425609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331714-A-G

168425610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331715-G-A

168426463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29339650-A-G

168426463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29339650-A-T

168426564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29339749-T-C

http://identifiers.org/hco/3/GRCh38#168426604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#29339804-C-A

168426738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29339928-G-T

http://identifiers.org/hco/3/GRCh38#168426806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29339993-C-A

168426955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340122-G-A

168426955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340122-G-C

168426959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340126-G-C

168427306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340229-C-T

168427342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340254-G-A

168427703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340407-T-C

168427739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29340442-G-A

168429439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342551-A-G

168429523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342638-C-G

168429523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342638-C-T

http://identifiers.org/hco/3/GRCh38#168429566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29342683-C-A

168429566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342683-C-T

168429575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342692-A-G

168429703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342806-G-T

168429739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342839-T-C

168429829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342907-T-G

http://identifiers.org/hco/3/GRCh38#168429884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29342961-A-C

168429886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29342963-G-A

168429988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343056-C-T

168429990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343058-A-G

168430031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343100-G-A

168430187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343250-C-T

168430431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343822-T-C

168430447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343838-T-C

168430513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343906-A-T

168432232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345000-G-A

168432378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345112-A-G

168432474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345188-G-C

168432474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345188-G-T

168432746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345436-G-A

168432746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345436-G-C

http://identifiers.org/hco/3/GRCh38#168432759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29345449-C-A

168432759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345449-C-T

168432812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345502-A-T

168432966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345709-C-G

168433114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345842-G-A

168433212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345943-G-A

168433305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346032-C-G

168433725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346517-C-T

168433726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346518-A-T

168433960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346747-A-G

168434301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347033-G-T

168434421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347154-G-A

http://identifiers.org/hco/3/GRCh38#168434470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29347203-A-C

168434517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347250-G-A

168434517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347250-G-T

168434623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347344-G-A

168434759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347459-G-A

168434808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347507-G-T

168434845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347537-T-A

168434864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347548-A-G

168435122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347785-A-G

168435237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29347899-T-C

168435590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348198-G-A

168438437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29350043-A-G

168438451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29350057-A-G

168439038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351789-G-A

168439614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352290-G-T

168439703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352381-A-G

168439777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352449-T-C

168439851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352548-A-G

168439858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352555-A-G

168439860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352557-A-G

168439861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352558-T-C

168440337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354627-T-C

168440379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354669-T-A

168440420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354711-C-T

168440437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354728-T-G

168440471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354761-T-G

http://identifiers.org/hco/3/GRCh38#168440559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29354856-C-A

168440559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354856-C-T

168440658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354955-A-G

168440658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354955-A-T

http://identifiers.org/hco/3/GRCh38#168440689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29354983-C-A

168440696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29354990-G-A

168440739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355036-T-C

http://identifiers.org/hco/3/GRCh38#168440836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29355137-A-C

168440836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355137-A-G

168440982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355233-G-T

168441083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355297-G-A

168441083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355297-G-C

168441170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355387-G-A

168441739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29356697-T-G

168441869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29356814-C-G

168441957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29356904-T-C

168442162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357096-A-T

168442181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357115-T-A

168442296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357245-A-G

168442296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357245-A-T

168442304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357253-A-T

168442341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357290-G-A

168442560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357499-T-C

http://identifiers.org/hco/3/GRCh38#168442640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29357563-A-C

168442640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357563-A-G

168442663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357586-T-C

168442668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357591-G-A

168442718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357644-C-T

168442857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357780-A-G

168444056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359161-G-A

168444134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359249-T-C

168444211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359333-T-C

168444603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359703-A-T

168444689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359787-C-T

168444785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359884-T-C

168444821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359920-T-C

168444980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360147-A-G

http://identifiers.org/hco/3/GRCh38#168445018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29360185-C-A

168445294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360504-C-T

168445391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360593-C-T

168445441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360639-C-T

http://identifiers.org/hco/3/GRCh38#168445499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29360704-A-C

168445563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360770-T-G

168445828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29361042-G-A

168447292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29361757-T-C

168447446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29361997-C-G

168447491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362040-T-C

168447525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362073-G-A

168447552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362100-T-C

168447560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362108-A-G

168447570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362118-A-T

168447740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362275-G-A

168447741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362276-T-G

http://identifiers.org/hco/3/GRCh38#168447784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29362319-A-C

168447784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362319-A-G

168447997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362533-C-T

168448141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362655-T-C

168448360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362842-C-T

168448451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362960-C-G

168448580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363076-C-T

168448765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363319-C-T

168448891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363470-T-A

168449084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363646-A-G

168449117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363677-A-G

168449171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363733-A-T

168449265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363822-A-G

168449269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363826-A-G

168449467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363945-G-A

168449520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29364000-C-T

168449734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29365748-T-C

168449760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29365774-A-G

168449959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29365936-T-C

168450029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29365988-T-C

168450031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29365990-G-C

168450549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366134-G-A

168450705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366266-G-A

168450705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366266-G-T

168451033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366608-G-A

168451065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366639-T-G

http://identifiers.org/hco/3/GRCh38#168451728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29366994-A-C

168451728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29366994-A-T

168451794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367063-G-A

168451950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367205-G-A

168452049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367283-A-G

168452849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367674-T-C

168452928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367758-G-A

168452941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367771-C-T

168452972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367802-A-G

168453210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368121-T-C

168453245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368266-C-T

168454724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375754-G-T

http://identifiers.org/hco/3/GRCh38#168454742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29375773-C-A

168454761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375793-T-G

168454860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375902-A-G

168454901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375935-A-G

168455097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376033-G-A

168455171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376087-A-G

168455231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376151-C-G

http://identifiers.org/hco/3/GRCh38#168455356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29376192-A-C

168455444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376260-A-G

168455530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376345-G-A

168457340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376505-C-T

168457362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376528-A-G

168457518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376680-A-G

168457600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376757-G-T

168457933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377089-T-G

168458016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377176-G-A

168458063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377217-T-A

168458327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377474-G-A

168458483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377514-C-T

168458492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377517-C-T

168458495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377520-C-T

168458519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377543-T-A

168458712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377737-A-G

http://identifiers.org/hco/3/GRCh38#168459133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29378071-C-A

168459190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378117-G-A

168459196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378123-G-A

168465767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379076-T-C

168465895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379209-C-G

168466184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379470-A-G

168467172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379862-A-T

168467448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380074-C-T

http://identifiers.org/hco/3/GRCh38#168468528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29380897-A-C

168468934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381270-G-T

168469023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381383-T-C

168469200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29382909-G-T

168469256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29382966-G-A

http://identifiers.org/hco/3/GRCh38#168469357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29383068-A-C

168469577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383252-G-T

168469669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383353-C-T

168469939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383698-G-A

168469993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383756-C-T

http://identifiers.org/hco/3/GRCh38#168470152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29383995-A-C

168470152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383995-A-G

168470420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384324-A-T

168470600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384490-T-G

168470686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384560-C-T

168470701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384575-G-T

168471065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385013-G-C

168471078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385026-T-C

http://identifiers.org/hco/3/GRCh38#168471113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29385061-C-A

168471113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385061-C-T

168471133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385081-G-A

168471141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385087-C-T

168471379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385299-T-G

168471641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385500-G-A

168471641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385500-G-T

168472554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385758-A-T

168472555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385759-T-G

168472603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385803-A-G

168472626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385825-C-T

168472627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385826-A-G

168472821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385954-T-C

168473167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386262-A-G

168473185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386280-T-C

168473209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386306-T-A

168473209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386306-T-C

168473282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386381-C-G

168473304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386403-A-G

168476131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389636-T-A

168476135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389640-C-T

168476224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389706-C-T

168476363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389844-C-T

168476729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390242-G-A

168476924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390435-A-G

168476928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390439-G-T

168477419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390884-C-G

168477419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390884-C-T

168477441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390899-A-T

168477512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390964-T-C

168477557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391123-A-G

168477680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391352-A-G

168477888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391518-T-C

168478008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391638-C-G

http://identifiers.org/hco/3/GRCh38#168478379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29391898-C-A

168478731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392246-A-G

168478732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392247-G-A

168478806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392321-T-G

168478809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392324-G-A

168478861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392374-T-C

168479724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392924-A-G

http://identifiers.org/hco/3/GRCh38#168479758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29392958-C-A

168479941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29393109-A-G

168483736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29394335-C-T

168484059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29394612-T-C

168484065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29394618-G-A

http://identifiers.org/hco/3/GRCh38#168484277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29394842-A-C

168484470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395035-C-G

168484830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395395-G-C

168484830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395395-G-T

168485455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396002-G-A

168485558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396036-A-G

168486045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396413-T-C

168486414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396790-A-G

http://identifiers.org/hco/3/GRCh38#168486643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29397096-A-C

168486692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397145-T-C

168486870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397360-C-T

168487124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397601-G-A

168487137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397614-C-T

168487161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397641-A-G

168487240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397719-A-G

168487344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397814-C-T

168487366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397831-A-T

168487676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398068-A-T

168487767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398159-T-C

168488096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398689-G-A

168488233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398814-G-A

168488295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398869-G-A

168488456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399024-C-T

168488488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399060-G-A

168488519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399089-G-T

168488527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399097-C-T

http://identifiers.org/hco/3/GRCh38#168488899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29399679-C-A

168488899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399679-C-G

168489115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399934-G-A

http://identifiers.org/hco/3/GRCh38#168489258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29400057-C-A

http://identifiers.org/hco/3/GRCh38#168489351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29400130-A-C

168489670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400445-C-T

http://identifiers.org/hco/3/GRCh38#168489783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29400550-C-A

168489783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400550-C-G

168489791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400558-C-G

168489845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400607-C-T

168489882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400646-A-G

168489883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400647-C-T

168491131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401069-A-G

http://identifiers.org/hco/3/GRCh38#168491355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29401276-C-A

168491368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401289-A-G

168491494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401421-A-T

168491614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401555-T-A

168491716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401659-A-G

168491865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401753-T-C

http://identifiers.org/hco/3/GRCh38#168492071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29402146-C-A

168492226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402264-C-T

168492368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402392-A-G

168492398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402405-T-C

168492648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402620-A-T

http://identifiers.org/hco/3/GRCh38#168492905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29402872-C-A

168492905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402872-C-T

168494532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410484-A-G

168494804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29410745-C-G

168495574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411505-T-A

168495790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411713-C-T

168495829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29411752-T-C

168497292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412865-C-T

168497312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412885-G-A

168497730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413302-C-G

168497882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413463-G-T

168498154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413721-G-A

168498212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29413761-G-A

168500089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414557-T-C

168500090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414558-G-A

168500146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414615-C-T

168500368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414853-T-C

http://identifiers.org/hco/3/GRCh38#168500615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29415064-A-C

168500615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415064-A-T

168501229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415580-A-G

168501323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415677-T-C

http://identifiers.org/hco/3/GRCh38#168501473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29415852-C-A

168501549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29415926-T-C

168501619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416023-A-G

168501646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416053-T-C

168501646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416053-T-G

168501942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416341-G-A

168506435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419495-C-G

168506535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419619-G-A

168506753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419828-A-G

168506820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29419889-A-G

168507259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420026-G-T

168507531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420303-A-G

168507612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420373-C-T

168507614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420375-C-T

168507694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420456-G-A

168507796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420556-A-G

168507894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29420652-A-G

http://identifiers.org/hco/3/GRCh38#168507977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29420738-C-A

168508669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421120-G-T

168508761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421213-A-G

168508865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421318-G-A

168508909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421361-G-A

168509024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421476-G-T

http://identifiers.org/hco/3/GRCh38#168509478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29421885-C-A

168509636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422008-T-C

168509637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422009-G-T

168509681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422036-C-T

168509770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422094-C-T

168509966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422222-T-A

168509998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422249-G-T

168510464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423577-T-C

168510615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423701-A-G

168510615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423701-A-T

168510935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29424089-C-T

168510966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29424119-A-G

168511106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29424263-T-C

168511299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29424565-C-T

168511747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29424992-C-T

168511901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29425494-A-G

168511927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29425537-C-T

168512191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29425820-G-A

168512308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29425928-G-A

168512854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29426559-A-G

168513367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427463-A-G

168513380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427476-A-G

168513409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427500-C-T

168513430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427521-G-A

168513470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427552-G-C

168513482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427564-C-T

168513564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427639-C-T

168513810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431246-A-G

168513864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431300-A-G

168513920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431355-G-A

168513920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431355-G-C

168514335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431857-A-G

168514339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431861-T-G

168514424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431958-T-C

168514483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432016-A-G

168514568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432111-A-G

168514568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432111-A-T

http://identifiers.org/hco/3/GRCh38#168514637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29432179-C-A

168514637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432179-C-G

http://identifiers.org/hco/3/GRCh38#168515466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29433065-A-C

168515466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433065-A-G

168515469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433068-T-C

168515480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433079-G-A

168515501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433095-G-C

168515558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433136-T-C

168515587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433165-A-G

168515587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433165-A-T

168515615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433193-T-C

168515629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433207-G-T

http://identifiers.org/hco/3/GRCh38#168515680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29433247-C-A

168515739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433285-A-T

168516144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434287-T-G

168516200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434328-A-G

http://identifiers.org/hco/3/GRCh38#168516224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#29434338-A-C

168516420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434531-A-G

168516502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434612-A-G

168516585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434694-A-G

168516683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434793-G-A

168516706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434816-G-A

168516829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434956-A-G

168516913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435038-G-C

168516993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435114-G-T

168517091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435209-C-G

168517241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435356-A-G

168517675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25149
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29435785-T-C