168834180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68991367-A-G

168834189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68991376-T-C

168834372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991559-G-A

168834375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991562-T-C

168834402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991587-G-A

168834416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991600-C-T

168834744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991710-G-A

168834863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991802-T-C

168835067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991999-T-C

168835592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992227-G-A

168835704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992345-G-C

168835745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992384-G-A

168835949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992552-T-C

168836432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993052-C-T

168836499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993126-G-T

168836633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993251-T-A

168836642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993260-C-T

168836644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993262-C-T

168836827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993365-C-T

168836838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993376-A-G

168837651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993970-C-G

168837806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994072-T-G

168837867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994132-A-G

168838097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994363-A-G

http://identifiers.org/hco/2/GRCh38#168838221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68994456-A-C

168838221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994456-A-T

168840195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994861-G-C

168840556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994903-A-G

168840693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995025-G-A

168840772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995106-G-A

168840772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995106-G-T

168841490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995428-G-A

168841490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995428-G-C

168842358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995617-T-C

168842451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68995712-T-C

168842924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996158-T-C

168843087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68996321-A-T

http://identifiers.org/hco/2/GRCh38#168843157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68996389-C-A

168843157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996389-C-T

http://identifiers.org/hco/2/GRCh38#168843183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68996415-C-A

168843384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996605-T-C

168843464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996674-C-T

168843758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997507-G-C

168843837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997587-T-C

168843947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997740-T-G

168843999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997788-G-A

168844270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68998039-G-A

168844377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68998618-C-T

168844679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68998758-G-C

168845167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999442-A-G

168845280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999524-C-T

168845449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999660-G-T

168845578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999791-T-A

168845702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000099-A-G

168845808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000163-G-A

168845808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000163-G-C

168845808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000163-G-T

168845828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000184-G-T

168845874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000229-T-C

168845901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000249-A-G

168846046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000374-C-T

168846158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000475-T-A

168847281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000559-T-G

http://identifiers.org/hco/2/GRCh38#168847517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69000762-A-C

168848020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001237-G-A

168848110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001338-G-C

168848180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001384-G-A

168848180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001384-G-T

168848333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001547-T-A

168848333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001547-T-G

168848566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001776-A-T

168848827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001983-T-G

168849084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002211-G-C

168849710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002352-G-A

168849761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002403-C-G

168849843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002463-C-T

http://identifiers.org/hco/2/GRCh38#168849858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69002478-C-A

http://identifiers.org/hco/2/GRCh38#168850269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69002629-C-A

http://identifiers.org/hco/2/GRCh38#168850277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69002637-C-A

http://identifiers.org/hco/2/GRCh38#168850334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69002693-C-A

168850388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002748-G-T

168850444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002797-C-G

http://identifiers.org/hco/2/GRCh38#168850576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69005536-A-C

http://identifiers.org/hco/2/GRCh38#168850577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69005537-C-A

http://identifiers.org/hco/2/GRCh38#168850618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69005600-A-C

168850618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005600-A-G

168850618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005600-A-T

168850619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005601-A-T

168850834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 69005616-A-G

168850893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005675-G-A

168850893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005675-G-T

http://identifiers.org/hco/2/GRCh38#168850909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69005711-A-C

168850909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005711-A-G

168850909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005711-A-T

168850920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005722-T-A

168850920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005722-T-C

168850920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005722-T-G

168850999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69005794-G-A

http://identifiers.org/hco/2/GRCh38#168851049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69005820-C-A

168851049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005820-C-T

168851208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005971-C-T

168851217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69005981-C-G

168851256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69006024-T-C

168853241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008110-C-T

168854619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008618-C-G

168854660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008657-C-G

http://identifiers.org/hco/2/GRCh38#168854850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69008796-C-A

168854864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008808-C-G

168854931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008870-C-T

http://identifiers.org/hco/2/GRCh38#168854969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69008908-A-C

168855043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008986-A-G

168855297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009252-G-A

168855297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009252-G-T

168855519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010006-A-G

http://identifiers.org/hco/2/GRCh38#168855541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010028-C-A

168855541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010028-C-T

168855542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010029-T-C

168855561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010050-T-C

168855583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010067-T-A

http://identifiers.org/hco/2/GRCh38#168855639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010467-A-C

168855693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010521-A-G

168855747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010573-G-A

168855768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010597-G-T

168855769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010598-T-A

168855838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010643-G-T

168855843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010648-T-C

168855854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010659-T-C

168855887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 69010692-A-T

http://identifiers.org/hco/2/GRCh38#168855903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010708-C-A

168855903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010708-C-G

http://identifiers.org/hco/2/GRCh38#168855939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010743-A-C

http://identifiers.org/hco/2/GRCh38#168855948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010752-C-A

168855950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010754-T-C

168856137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010911-T-C

168856161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010933-A-G

http://identifiers.org/hco/2/GRCh38#168856194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010966-A-C

168856194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010966-A-G

http://identifiers.org/hco/2/GRCh38#168856286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69010994-C-A

168856286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010994-C-T

168856291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69010999-T-A

168856464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011061-A-G

168856606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 69011092-G-A

168856606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 69011092-G-T

168856626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011112-G-A

168856626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011112-G-C

168856626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011112-G-T

http://identifiers.org/hco/2/GRCh38#168856643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69011128-C-A

168856647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011132-G-C

168856653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011138-G-A

168856685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 69011170-T-C

http://identifiers.org/hco/2/GRCh38#168856692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69011177-C-A

168856863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011338-G-T

168856883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011358-G-T

168857052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011476-T-A

168857052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011476-T-C

168857052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69011476-T-G

http://identifiers.org/hco/2/GRCh38#168857112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69011533-C-A

168857766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012380-C-T

168857893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012505-A-T

168858015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012630-C-T

168858016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012631-C-G

168858016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012631-C-T

168858017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012632-C-T

168858111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012726-A-T

168858263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69012897-T-C

168859448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69013102-T-G

http://identifiers.org/hco/2/GRCh38#168859524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69013183-C-A

168859524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69013183-C-T

168859559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69013218-A-G

168859658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69013318-T-C

168859673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69013334-T-C

168859674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69013335-G-A

168859924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69013574-A-T

168860125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69013875-G-A

168860542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014119-G-A

http://identifiers.org/hco/2/GRCh38#168860686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69014139-A-C

168860686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014139-A-G

168860686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014139-A-T

168860879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69014309-G-T

168861051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014479-G-A

168861051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014479-G-T

http://identifiers.org/hco/2/GRCh38#168861061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69014489-C-A

168861061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014489-C-G

168861061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014489-C-T

168861095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69014525-A-G

168861635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015427-C-G

http://identifiers.org/hco/2/GRCh38#168861655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69015447-A-C

168861810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015668-A-G

168862064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015907-C-T

168862088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015931-A-G

http://identifiers.org/hco/2/GRCh38#168862129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69015972-C-A

http://identifiers.org/hco/2/GRCh38#168862158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69015998-C-A

168862158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015998-C-G

168862158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69015998-C-T

168862373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016215-A-G

168862446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016288-T-C

168862548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016388-G-A

168862690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016511-G-A

168862690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016511-G-C

168862912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016789-C-T

168862928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69016879-G-A

http://identifiers.org/hco/2/GRCh38#168862989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69017056-A-C

168862989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69017056-A-T

http://identifiers.org/hco/2/GRCh38#168863193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69017240-C-A

168863193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69017240-C-G

168863206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69017253-G-A

168863593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69018834-A-G

168863728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69018973-A-T

http://identifiers.org/hco/2/GRCh38#168863741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69018985-A-C

http://identifiers.org/hco/2/GRCh38#168863807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019036-C-A

168863847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019072-C-T

http://identifiers.org/hco/2/GRCh38#168863863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019078-A-C

168863863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019078-A-G

168864751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019249-G-A

168864751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019249-G-T

168864773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019274-A-G

168864823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019330-T-G

http://identifiers.org/hco/2/GRCh38#168864848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019355-A-C

168864848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019355-A-G

168864848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019355-A-T

168865020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019528-T-A

168865020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019528-T-C

168865020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019528-T-G

168865034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019542-G-A

168865034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019542-G-C

168865034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69019542-G-T

168865083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019590-T-C

http://identifiers.org/hco/2/GRCh38#168865200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019697-C-A

168865241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019726-G-A

168865241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019726-G-T

168865252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019737-A-G

168865293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019756-T-G

168865362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019830-G-A

168865362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019830-G-C

http://identifiers.org/hco/2/GRCh38#168865375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019843-C-A

168865375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019843-C-T

168865385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019852-G-A

168865385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019852-G-T

168865390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69019857-G-A

168865390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69019857-G-C

168865390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69019857-G-T

http://identifiers.org/hco/2/GRCh38#168865425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019896-C-A

168865425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019896-C-G

168865436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019910-A-G

http://identifiers.org/hco/2/GRCh38#168865445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69019919-C-A

168865445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69019919-C-T

168871542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69024876-G-A

168871542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69024876-G-C

168871542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69024876-G-T

168871594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024926-T-A

168871623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024952-T-C

168871632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024958-T-C

http://identifiers.org/hco/2/GRCh38#168871654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69024980-C-A

168871654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024980-C-G

168871859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025183-A-G

168872278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025952-A-T

168872364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026026-T-A

168872426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026086-C-T

http://identifiers.org/hco/2/GRCh38#168872431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69026091-A-C

168872599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026271-G-T

http://identifiers.org/hco/2/GRCh38#168873056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69027050-A-C

168873104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027086-A-G

168873296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027223-G-C

168873355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027281-T-C

168873370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027296-C-G

http://identifiers.org/hco/2/GRCh38#168873555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69027455-A-C

168873701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027599-T-G

http://identifiers.org/hco/2/GRCh38#168873742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69027717-A-C

168873742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027717-A-G

168873753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027728-G-T

168873772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027745-A-G

168873800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69027765-T-C

http://identifiers.org/hco/2/GRCh38#168873802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69027767-C-A

168875756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030012-A-G

168875985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030252-G-A

168875985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030252-G-T

http://identifiers.org/hco/2/GRCh38#168876040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69030302-C-A

168876040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030302-C-G

168876040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030302-C-T

168876064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69030321-A-G

168876082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69030339-T-C

168876118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69030375-T-C

168876118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69030375-T-G

168876223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030477-A-G

http://identifiers.org/hco/2/GRCh38#168876281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69030536-C-A

168876281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030536-C-G

http://identifiers.org/hco/2/GRCh38#168876287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69030542-A-C

168876287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030542-A-T

168876457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030655-T-C

168876587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030815-A-T

168876588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030816-G-T

168876746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030943-T-C

168877086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69032776-A-T

http://identifiers.org/hco/2/GRCh38#168877188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69032864-C-A

168877203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69032892-A-G

168877243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69032921-T-C

168877283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69032961-C-T

168877347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69033025-C-G

http://identifiers.org/hco/2/GRCh38#168877517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69033288-C-A

168877525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033296-T-A

168878159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033595-A-G

168889131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035117-T-C

http://identifiers.org/hco/2/GRCh38#168889140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69035126-A-C

168889148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035134-G-A

168889213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035186-C-T

168889240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69035214-A-G

http://identifiers.org/hco/2/GRCh38#168889248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69035222-C-A

168889253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69035227-C-G

168889322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035302-T-G

168889364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035344-T-C

168889380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69035361-T-G

168889393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69035376-A-G

168889418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69035401-A-G

168889493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69035482-G-A

168889493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69035482-G-C

168890059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036121-G-A

168890174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036226-C-T

168890204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036271-A-G

168890270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036357-T-C

http://identifiers.org/hco/2/GRCh38#168890277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69036364-A-C

168890277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036364-A-G

168890277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036364-A-T

168890284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036371-C-G

168890284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036371-C-T

168890336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036422-G-C

168890336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036422-G-T

http://identifiers.org/hco/2/GRCh38#168890343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69036429-C-A

168890343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036429-C-G

168890343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036429-C-T

168890350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036436-C-T

http://identifiers.org/hco/2/GRCh38#168890358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69036444-A-C

168890358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036444-A-G

168890359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036445-G-A

168890359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036445-G-C

168890359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036445-G-T

168890363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036449-C-T

168890370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036455-A-G

168890376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036461-G-A

168890376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036461-G-C

168890376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69036461-G-T

168890405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69036498-C-T

http://identifiers.org/hco/2/GRCh38#168890435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69036535-C-A

168890470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036564-G-A

168890470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036564-G-T

168890473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036567-G-A

168890473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036567-G-T

http://identifiers.org/hco/2/GRCh38#168890476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69036570-C-A

168890532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69036628-T-G

168890598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69036690-G-T

168890689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69036739-G-T

168890876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036942-T-A

168891607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039798-G-T

http://identifiers.org/hco/2/GRCh38#168894692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69045594-C-A

168894736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69045638-T-G

168894802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69045706-G-T

168895121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69046012-G-A

http://identifiers.org/hco/2/GRCh38#168895473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69046370-A-C

168895571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69046455-G-T

168895730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69046899-A-G

168895908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69047115-G-T

168899145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69047742-T-G

168899256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69047868-T-C

168899456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048012-A-G

168899629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048211-C-T

168899768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048350-C-T

168899897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048474-T-G

168899908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048485-C-T

168900556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69049294-G-A

168900556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69049294-G-T

168900637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69049366-T-A

168900748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69049806-T-G

168900828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69049889-C-T

168901071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69050139-T-C

168901129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69050179-G-A

http://identifiers.org/hco/2/GRCh38#168901244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050295-C-A

168901245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69050296-A-G

http://identifiers.org/hco/2/GRCh38#168901293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050344-C-A

168901293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050344-C-T

http://identifiers.org/hco/2/GRCh38#168901402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050447-C-A

168901505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050550-A-G

168901505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69050550-A-T

http://identifiers.org/hco/2/GRCh38#168901513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050558-C-A

168901513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050558-C-T

168901622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050661-A-G

168901670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050708-G-T

http://identifiers.org/hco/2/GRCh38#168901683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050721-C-A

168901683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050721-C-T

168902138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050840-T-A

http://identifiers.org/hco/2/GRCh38#168902190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69050891-C-A

168902190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69050891-C-T

168902328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051005-C-T

168902354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051039-T-G

168902364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051049-T-C

168902414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051097-T-C

168902414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051097-T-G

http://identifiers.org/hco/2/GRCh38#168902505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69051187-C-A

168902505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69051187-C-T

168902541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 69051223-T-A

168902541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69051223-T-C

168902800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051467-T-A

168902806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051473-C-G

168902806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051473-C-T

168903014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051695-T-A

168903018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051699-G-T

168903034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051715-T-C

168903095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051777-G-A

168903095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051777-G-T

168903096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051778-G-A

168903096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051778-G-T

168903295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69051978-C-T

168903392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052057-C-T

168903521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052163-T-C

168903534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052176-A-T

168903730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052313-T-C

168903785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052369-C-G

168903785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052369-C-T

168903787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052371-A-G

168903893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052502-C-G

168903934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052540-C-T

168904222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052956-G-A

168904232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69052966-G-T

168904304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053108-T-A

168904355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053159-C-G

168904376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053180-A-G

http://identifiers.org/hco/2/GRCh38#168904436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69053211-A-C

168904436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053211-A-G

168904436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053211-A-T

http://identifiers.org/hco/2/GRCh38#168904530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69053301-C-A

168904530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69053301-C-G

168904530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69053301-C-T

168904539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 69053310-T-A

168904604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053375-T-C

168904645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053405-T-A

168904676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053434-T-G

168904925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69053688-A-G

168905913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055057-C-T

168905941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055087-G-T

168905958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055096-T-A

http://identifiers.org/hco/2/GRCh38#168906024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69055154-C-A

http://identifiers.org/hco/2/GRCh38#168906052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69055174-C-A

168906052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055174-C-T

http://identifiers.org/hco/2/GRCh38#168906135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69055207-C-A

168906295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055374-T-C

168906490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69055995-T-C

http://identifiers.org/hco/2/GRCh38#168906518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69056011-C-A

168906518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056011-C-T

http://identifiers.org/hco/2/GRCh38#168906534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69056028-A-C

168906534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056028-A-G

168906559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056050-C-T

168906583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056074-G-A

168906583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056074-G-T

168906623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056115-T-G

http://identifiers.org/hco/2/GRCh38#168906858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69056346-C-A

168906858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056346-C-G

168906858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056346-C-T

168906875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056361-A-G

http://identifiers.org/hco/2/GRCh38#168906919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69056404-C-A

168906919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056404-C-T

168907012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056505-T-C

168907108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056581-T-G

168907228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056628-A-G

168907416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056786-T-G

168907434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056803-G-C

168907434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056803-G-T

http://identifiers.org/hco/2/GRCh38#168907451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69056820-C-A

168907453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69056822-G-T

168907716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69057060-C-T

168907773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 69057117-G-A

168907873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057217-T-C

168907873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057217-T-G

168907879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057223-C-G

168907957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057301-G-A

168907957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057301-G-C

http://identifiers.org/hco/2/GRCh38#168907997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057341-C-A

http://identifiers.org/hco/2/GRCh38#168908034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057378-C-A

168908071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057415-A-G

http://identifiers.org/hco/2/GRCh38#168908108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057444-C-A

168908108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057444-C-T

168908137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057476-G-T

168908337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057640-G-A

168908422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057726-T-C

http://identifiers.org/hco/2/GRCh38#168908433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057737-C-A

http://identifiers.org/hco/2/GRCh38#168908442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057745-C-A

168908442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057745-C-T

http://identifiers.org/hco/2/GRCh38#168908491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057796-C-A

168908592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057923-G-C

168908592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057923-G-T

168908597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057928-A-G

168908608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 69057939-A-G

http://identifiers.org/hco/2/GRCh38#168908631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69057961-C-A

168909115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69058078-T-C

http://identifiers.org/hco/2/GRCh38#168909157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69058120-C-A

http://identifiers.org/hco/2/GRCh38#168909666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69058465-C-A

168909720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69058509-A-G

168909943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69058730-T-G

168910147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69058881-G-T

168910280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69059010-T-C

168910350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69059068-G-A

168910350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69059068-G-T

168910416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69059136-T-C

168910651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69059371-C-T

http://identifiers.org/hco/2/GRCh38#168910937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69059633-C-A

168911418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060019-C-T

168911638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69060108-G-A

168911676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69060167-A-G

168911677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69060168-A-G

168911700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69060191-G-T

168911902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060370-G-A

168911996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060451-T-C

168912164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060612-G-C

168912212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060651-G-A

168912218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060657-C-T

168912427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69060855-G-A

168912952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69061342-G-A

http://identifiers.org/hco/2/GRCh38#168912995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24031
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69061385-C-A