18871479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3 prime UTR variant
orthologous variants: 139376517-A-T

18871499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3 prime UTR variant
orthologous variants: 139376498-T-C

18871607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3 prime UTR variant
orthologous variants: 139376415-T-C

18871634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3 prime UTR variant
orthologous variants: 139376393-G-A

18871634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3 prime UTR variant
orthologous variants: 139376393-G-T

18872001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376250-G-A

http://identifiers.org/hco/1/GRCh38#18872003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139376248-C-A

18872003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376248-C-T

http://identifiers.org/hco/1/GRCh38#18872109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139376214-C-A

18872121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376201-T-C

18872121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376201-T-G

http://identifiers.org/hco/1/GRCh38#18872145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139376180-C-A

18872145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376180-C-G

18872145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376180-C-T

18872337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376060-G-A

18872337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376060-G-T

18872363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376037-G-A

18872363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376037-G-T

18872376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376024-T-C

18872387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376013-G-A

18872387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139376013-G-T

http://identifiers.org/hco/1/GRCh38#18872413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139375993-A-C

18872413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375993-A-T

18872430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375977-T-C

18872444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375963-T-A

18872444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375963-T-C

18872444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375963-T-G

18872554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375864-A-G

18872578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375836-G-C

18872608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375802-A-G

18872620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375792-G-A

18872620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375792-G-T

http://identifiers.org/hco/1/GRCh38#18872621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139375791-C-A

18872621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375791-C-G

18872621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375791-C-T

18872637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375772-T-G

18872752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375669-T-A

18872752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375669-T-C

18872752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375669-T-G

18872755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375666-A-G

18872755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375666-A-T

18872763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375658-T-C

18872763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 139375658-T-G

18872915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139375509-C-G

18872915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: stop gained
orthologous variants: 139375509-C-T

http://identifiers.org/hco/1/GRCh38#18872961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139375463-C-A

18872961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139375463-C-T

18874104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372701-G-A

18874221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372585-A-G

18874277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372538-A-T

18874317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372499-G-A

18874319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372497-A-G

18874329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372489-A-T

18874342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372476-G-A

18874342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372476-G-T

http://identifiers.org/hco/1/GRCh38#18874348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139372470-C-A

http://identifiers.org/hco/1/GRCh38#18874372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139372453-C-A

18874372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372453-C-T

18874378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372447-T-A

18874378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372447-T-C

http://identifiers.org/hco/1/GRCh38#18874404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139372433-A-C

18874404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372433-A-G

18874434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372422-C-T

http://identifiers.org/hco/1/GRCh38#18874480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139372389-C-A

18874480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139372389-C-G

18874480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139372389-C-T

18874561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139372308-G-A

18874577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139372292-C-T

18874625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372258-C-T

http://identifiers.org/hco/1/GRCh38#18874696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139372191-C-A

18874696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372191-C-G

18874696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372191-C-T

18874795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139372078-C-T

18874885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371985-C-T

18874963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371926-C-T

18875070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371820-C-T

18875245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371685-C-T

18875257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139371673-G-T

http://identifiers.org/hco/1/GRCh38#18875307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139371618-C-A

18875307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371618-C-T

18875326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139371599-G-T

18875343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139371582-C-T

18875430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, undefined
orthologous variants: 139371494-T-A

18875526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371408-A-G

18875566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371392-C-G

http://identifiers.org/hco/1/GRCh38#18875572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139371386-C-A

18875572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371386-C-T

18875618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139371343-C-T

18875639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371323-G-A

18875639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371323-G-T

18875662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139371297-G-A

18875691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371272-T-A

18875691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371272-T-C

18875788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139371200-C-T

18876177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370937-G-A

18876177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370937-G-T

18876181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370933-G-C

18876181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370933-G-T

18876187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370927-T-A

18876187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370927-T-C

18876264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370877-G-A

18876264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370877-G-T

http://identifiers.org/hco/1/GRCh38#18876268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139370873-C-A

18876268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370873-C-T

18876302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370864-C-G

18876358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant
orthologous variants: 139370808-C-T

18876421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant
orthologous variants: 139370745-G-A

18876454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant
orthologous variants: 139370712-A-G

18876473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139370693-G-A

18876473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139370693-G-C

18876473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139370693-G-T

http://identifiers.org/hco/1/GRCh38#18876579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139370589-A-C

18876595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370575-G-T

18876771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370402-T-A

18876908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370129-G-A

http://identifiers.org/hco/1/GRCh38#18876948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139370070-C-A

18876948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139370070-C-T

18877074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369961-G-T

18877212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139369866-G-A

http://identifiers.org/hco/1/GRCh38#18877298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139369770-C-A

18877298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369770-C-T

http://identifiers.org/hco/1/GRCh38#18877522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139369476-C-A

18877525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139369473-T-C

http://identifiers.org/hco/1/GRCh38#18877585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139369413-A-C

18877622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369376-T-A

18877622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369376-T-C

18877622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369376-T-G

http://identifiers.org/hco/1/GRCh38#18877688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139369334-A-C

18877688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369334-A-G

18877688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369334-A-T

18877730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369303-C-T

http://identifiers.org/hco/1/GRCh38#18877933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139369154-A-C

18878006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369102-G-A

18878032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139369094-C-T

18878264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368897-C-G

18878348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368831-C-T

18878469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368715-T-A

18878611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368583-A-G

18878802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368399-G-A

18878826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368376-A-G

18878856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368346-T-C

18879005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368249-G-A

http://identifiers.org/hco/1/GRCh38#18879123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139368154-A-C

http://identifiers.org/hco/1/GRCh38#18879152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139368147-C-A

18879152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368147-C-T

18879178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368104-T-G

18879250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368034-G-T

18879252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368032-G-A

18879253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368031-A-G

18879253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368031-A-T

18879280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368004-G-A

http://identifiers.org/hco/1/GRCh38#18879295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139368000-C-A

18879295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139368000-C-T

http://identifiers.org/hco/1/GRCh38#18879374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367921-C-A

18879374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: splice acceptor variant
orthologous variants: 139367921-C-T

http://identifiers.org/hco/1/GRCh38#18879410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367891-C-A

18879410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367891-C-T

18879418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367885-A-T

18879462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367845-G-A

18879462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367845-G-T

http://identifiers.org/hco/1/GRCh38#18879487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367806-C-A

18879487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367806-C-T

http://identifiers.org/hco/1/GRCh38#18879506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367787-C-A

18879506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367787-C-T

18879635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367704-T-C

18879742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367621-T-C

18879753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367610-C-G

18880021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367379-C-T

18880171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367241-C-G

18880175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367237-G-A

http://identifiers.org/hco/1/GRCh38#18880204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367211-C-A

18880285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367125-A-G

18880292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367118-C-G

http://identifiers.org/hco/1/GRCh38#18880402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139367028-C-A

18880402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367028-C-T

18880406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367024-A-G

18880432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139367004-G-A

http://identifiers.org/hco/1/GRCh38#18880591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139366865-C-A

18880605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366851-A-G

18880607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366849-C-G

18880812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366655-A-T

18880903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366580-T-C

18881015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366447-C-T

18881165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366321-T-C

18881274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366219-T-C

18881275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139366218-C-G

http://identifiers.org/hco/1/GRCh38#18881546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139366005-A-C

18881598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365955-G-A

18881598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365955-G-T

18881620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365933-G-A

18881620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365933-G-T

18881676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365897-C-T

18881678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365895-T-C

18881929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365640-C-G

18881929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365640-C-T

http://identifiers.org/hco/1/GRCh38#18881930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139365639-C-A

18881930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365639-C-T

http://identifiers.org/hco/1/GRCh38#18881947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139365620-C-A

18881947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365620-C-T

18882018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365574-T-A

18882018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365574-T-C

18882018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365574-T-G

18882042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365538-G-A

18882117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365471-C-T

18882486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365162-G-C

18882486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139365162-G-T

http://identifiers.org/hco/1/GRCh38#18882564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139365092-C-A

http://identifiers.org/hco/1/GRCh38#18882660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139365026-C-A

18882661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139365025-T-A

18882661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139365025-T-G

18882753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364939-T-C

18882794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364900-G-T

18882799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364895-G-A

18882976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364677-G-T

http://identifiers.org/hco/1/GRCh38#18882988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364665-C-A

18882988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364665-C-G

http://identifiers.org/hco/1/GRCh38#18883003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364654-A-C

18883003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139364654-A-G

18883137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364556-G-A

18883137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364556-G-C

18883161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364532-G-A

18883271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 139364424-G-A

http://identifiers.org/hco/1/GRCh38#18883283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364413-A-C

http://identifiers.org/hco/1/GRCh38#18883297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364399-C-A

18883297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139364399-C-T

18883298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364398-G-A

18883298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364398-G-T

http://identifiers.org/hco/1/GRCh38#18883319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364377-A-C

18883352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364344-G-A

18883352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364344-G-T

18883358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139364338-T-G

http://identifiers.org/hco/1/GRCh38#18883568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139364177-C-A

18884150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363989-T-C

18884336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139363864-A-G

18884346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139363854-A-G

18884481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363764-C-G

18884682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363659-G-A

http://identifiers.org/hco/1/GRCh38#18884709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139363634-C-A

18884709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363634-C-T

18884714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363629-G-A

18885077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363322-G-A

http://identifiers.org/hco/1/GRCh38#18885080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139363319-C-A

http://identifiers.org/hco/1/GRCh38#18885217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139363079-C-A

18885250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363046-G-A

18885250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363046-G-T

18885264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363033-A-G

18885266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363031-G-A

18885266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363031-G-T

18885279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139363018-T-A

http://identifiers.org/hco/1/GRCh38#18885318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362987-C-A

18885318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362987-C-G

18885318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362987-C-T

18885344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362969-G-A

http://identifiers.org/hco/1/GRCh38#18885347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362966-C-A

18885347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362966-C-T

http://identifiers.org/hco/1/GRCh38#18885360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362953-C-A

18885360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362953-C-T

18885382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362931-A-G

18885382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362931-A-T

18885383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362930-G-A

18885383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362930-G-T

http://identifiers.org/hco/1/GRCh38#18885384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362929-C-A

18885384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362929-C-T

18885385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362928-G-A

18885385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362928-G-T

18885403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362910-T-C

http://identifiers.org/hco/1/GRCh38#18885425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362892-A-C

18885425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362892-A-T

http://identifiers.org/hco/1/GRCh38#18885451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362874-C-A

18885451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139362874-C-T

http://identifiers.org/hco/1/GRCh38#18885483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362843-A-C

18885483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139362843-A-G

18885483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139362843-A-T

18885667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362658-G-A

18885667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362658-G-T

18885695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362645-G-A

http://identifiers.org/hco/1/GRCh38#18885725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139362620-C-A

18885725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362620-C-T

18885732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362613-G-A

18885732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362613-G-T

18885912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362526-T-C

18886050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362404-A-G

18886131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362279-A-G

18886368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139362069-A-G

18886468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant
orthologous variants: 139362016-T-A

http://identifiers.org/hco/1/GRCh38#18889270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139361372-C-A

18889270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139361372-C-T

http://identifiers.org/hco/1/GRCh38#18889275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139361367-C-A

18889275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139361367-C-T

http://identifiers.org/hco/1/GRCh38#18889365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139361295-C-A

18889365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: synonymous variant
orthologous variants: 139361295-C-G

18889365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: synonymous variant
orthologous variants: 139361295-C-T

18889380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: synonymous variant
orthologous variants: 139361280-G-A

18889380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139361280-G-T

18889399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139361261-T-C

18889417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139361243-G-C

18889417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: missense variant
orthologous variants: 139361243-G-T

http://identifiers.org/hco/1/GRCh38#18889427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#139361233-C-A

18890006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139361123-C-T

18890076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 139361053-T-G

18890082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 139361047-G-A

http://identifiers.org/hco/1/GRCh38#18890100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139361029-C-A

18890100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 139361029-C-G

18890100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 139361029-C-T

http://identifiers.org/hco/1/GRCh38#18890235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139360955-A-C

18890235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360955-A-G

http://identifiers.org/hco/1/GRCh38#18890289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139360925-C-A

http://identifiers.org/hco/1/GRCh38#18890290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139360924-C-A

18890631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360846-T-G

http://identifiers.org/hco/1/GRCh38#18890638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139360839-C-A

18890661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360816-T-G

18890776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 139360736-C-T

18890805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 139360711-G-C

18890826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 139360695-G-T

18890876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 139360648-G-A

18890876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 139360648-G-C

18890934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360596-G-A

18890934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360596-G-C

18890969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360560-T-C

18890970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360559-C-G

18891022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360528-T-A

18891022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360528-T-C

http://identifiers.org/hco/1/GRCh38#18891057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139360508-C-A

18891057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360508-C-T

18891200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360356-G-A

18891289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139360293-G-A

18894888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139358572-G-T

18896025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139356966-C-T

18896086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139356897-C-T

18896225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139356807-G-A

18900727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139352200-G-A

18900727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139352200-G-C

18900780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139352156-G-T

18900985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351982-T-C

18900985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351982-T-G

18901065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351888-G-A

18901143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351798-A-G

18901155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351785-A-G

18901381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351594-C-T

18901413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351560-G-A

18901426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, undefined
orthologous variants: 139351549-C-T

18901496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351442-C-T

18901766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351225-G-C

18901766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351225-G-T

18901836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351155-C-T

18901966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron variant
orthologous variants: 139351052-G-C

18902300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139350636-C-G

18902311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350625-T-A

18902311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350625-T-G

18902320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350607-A-G

18902320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350607-A-T

http://identifiers.org/hco/1/GRCh38#18902366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350562-C-A

18902366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139350562-C-G

18902366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139350562-C-T

http://identifiers.org/hco/1/GRCh38#18902367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350561-A-C

18902367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139350561-A-G

18902367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139350561-A-T

18902465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139350503-G-A

18902465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139350503-G-T

http://identifiers.org/hco/1/GRCh38#18902467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350501-C-A

18902467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139350501-C-T

http://identifiers.org/hco/1/GRCh38#18902468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350500-C-A

18902468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139350500-C-G

18902468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139350500-C-T

18902477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350491-G-A

http://identifiers.org/hco/1/GRCh38#18902498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350470-C-A

18902498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350470-C-G

18902498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350470-C-T

18902508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350463-G-A

18902508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350463-G-T

18902557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350402-T-A

18902557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350402-T-C

18902557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350402-T-G

http://identifiers.org/hco/1/GRCh38#18902563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#139350396-C-A

18902563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350396-C-G

18902563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350396-C-T

18902565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350394-G-A

18902565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350394-G-T

18902648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350311-G-A

18902648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350311-G-T

18902653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350306-G-A

18902653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350306-G-T

18902683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139350292-T-C