17787953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909063-A-T

17788045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909162-T-C

http://identifiers.org/hco/22/GRCh38#17788086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120909203-C-A

17788125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909240-C-T

17788126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909241-G-A

http://identifiers.org/hco/22/GRCh38#17788127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120909242-C-A

17788127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909242-C-T

17788180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909295-G-A

17788240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909359-G-T

17788281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909408-C-T

17788521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120909633-C-T

17788703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120909810-G-A

17788804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120909909-G-A

17788804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120909909-G-C

17788804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120909909-G-T

17788847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120909952-A-G

17788950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910011-A-G

17788950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910011-A-T

17788972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910033-G-A

17788972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910033-G-T

http://identifiers.org/hco/22/GRCh38#17789068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910098-C-A

17789068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910098-C-T

http://identifiers.org/hco/22/GRCh38#17789208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910221-C-A

17789286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910269-A-G

17789487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910420-G-A

17789487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910420-G-T

17789506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910437-G-A

17789512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910443-G-A

http://identifiers.org/hco/22/GRCh38#17789547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910482-C-A

17789547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910482-C-T

http://identifiers.org/hco/22/GRCh38#17789567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910502-C-A

17789567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910502-C-G

17789567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910502-C-T

http://identifiers.org/hco/22/GRCh38#17789583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910518-C-A

17789583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910518-C-T

17789695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910630-G-A

17789695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910630-G-T

17789799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910735-C-T

http://identifiers.org/hco/22/GRCh38#17789857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120910802-C-A

17789857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910802-C-T

17789956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910898-A-G

17789978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910931-G-A

17789978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120910931-G-T

17790141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911092-G-A

17790162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911113-T-C

17790220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911156-G-A

17790220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911156-G-T

17790238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911183-G-A

17790317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911247-G-A

17790436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911351-A-G

17790456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911371-G-A

17790456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911371-G-C

17790456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911371-G-T

17790575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911504-T-A

17790575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911504-T-C

17790575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911504-T-G

http://identifiers.org/hco/22/GRCh38#17790625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120911522-A-C

17790625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911522-A-G

17790666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911563-G-A

17790666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911563-G-T

http://identifiers.org/hco/22/GRCh38#17790683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120911580-C-A

17790683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911580-C-T

http://identifiers.org/hco/22/GRCh38#17790687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120911584-C-A

17790713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911612-T-C

17790726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911625-G-A

17790726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120911625-G-T

17790937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120911835-G-A

17790937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120911835-G-C

17790944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120911840-G-A

17790944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120911840-G-C

17790944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120911840-G-T

17791158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120912057-T-C

17791187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120912114-C-T

17791216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120912149-C-T

17791234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120912167-G-C

17791305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120912239-C-T

http://identifiers.org/hco/22/GRCh38#17791314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120912248-C-A

17791314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120912248-C-G

17791314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120912248-C-T

17791606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120912584-T-A

http://identifiers.org/hco/22/GRCh38#17791616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120912594-C-A

http://identifiers.org/hco/22/GRCh38#17791643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120912613-C-A

17791963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120912800-C-T

17792496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120913282-G-A

17793322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120914115-C-T

17793902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120914717-A-G

17794044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120914875-T-C

http://identifiers.org/hco/22/GRCh38#17794349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120915046-C-A

17794412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915112-G-C

17794665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915374-C-T

17794945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915650-G-T

17795025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915713-C-T

17795125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915825-C-G

17795130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915830-C-G

17795233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915898-C-G

17795233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915898-C-T

17795276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120915940-C-T

17795423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916108-A-G

17795455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916139-C-T

17795456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916140-G-A

17795766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916458-A-G

17795858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916548-G-C

17795869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916561-T-C

17795890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916583-T-G

17795905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916595-T-A

17795905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120916595-T-G

17797654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120917045-C-T

17797733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120917124-G-A

17799449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120918610-G-A

17799727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120918849-G-A

17799760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120918877-C-T

17799803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120918915-C-G

17799825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120918936-G-A

17799929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120919044-G-A

17799949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120919057-A-G

17799984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120919093-G-A

17800018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120919109-A-G

17800271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120919339-T-C

http://identifiers.org/hco/22/GRCh38#17800437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#120919715-A-C

17800437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120919715-A-T

17800461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120919742-G-T

17800901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120920327-T-C

17800942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120920379-G-C

17802395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120920768-C-T

17802416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120920789-C-T

17802440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120920816-G-A

17802533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120920904-T-C

17802568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120920939-G-A

17802770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120922557-C-T

17803269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120922943-G-C

17803295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120922964-T-A

17803295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120922964-T-C

17803297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120922966-G-A

17803342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923007-C-G

17803342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923007-C-T

17803399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923024-C-T

17803419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923037-G-C

17803420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923038-C-T

17803421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923039-G-A

17803421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923039-G-C

17803421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923039-G-T

17803424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923042-A-T

17803539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923172-C-T

17803549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923182-G-A

17803549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923182-G-T

17803591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120923238-A-G

17803627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120923273-G-T

17804010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923700-G-T

17804036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923722-A-G

17804078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923772-C-T

17804160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923857-C-T

17804199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120923895-T-G

17804667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120924320-A-T

17804892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120924508-C-G

17804986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120924587-G-A

17805009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120924608-C-T

17805046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120924645-C-T

http://identifiers.org/hco/22/GRCh38#17805235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120924804-C-A

17805521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120925018-T-C

http://identifiers.org/hco/22/GRCh38#17807192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120926580-C-A

17807306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120926690-T-C

http://identifiers.org/hco/22/GRCh38#17807339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120926731-C-A

17807339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120926731-C-T

17807864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927195-C-T

17807881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927212-G-C

17808003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927331-G-A

17808022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927352-C-G

17808102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927396-C-T

17808246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927636-T-G

17808513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927913-C-T

http://identifiers.org/hco/22/GRCh38#17808580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120927999-C-A

17808580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120927999-C-T

17808601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120928023-T-C

17808722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120928133-G-T

17808735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120928146-C-T

17808851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120928269-G-A

17808851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120928269-G-C

17808851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120928269-G-T

17808857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120928275-G-A

17808857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120928275-G-T

17808984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120928405-T-C

17810431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929061-G-C

http://identifiers.org/hco/22/GRCh38#17810503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929125-C-A

17810531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929153-G-A

17810531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929153-G-T

http://identifiers.org/hco/22/GRCh38#17810566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929201-C-A

17810566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929201-C-T

17810582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929217-G-A

17810582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929217-G-T

http://identifiers.org/hco/22/GRCh38#17810604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929242-C-A

17810604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929242-C-T

17810611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929253-G-A

17810611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120929253-G-T

http://identifiers.org/hco/22/GRCh38#17810677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929310-C-A

http://identifiers.org/hco/22/GRCh38#17810678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929311-C-A

17810695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120929323-G-A

17810899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929529-G-C

17810899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929529-G-T

http://identifiers.org/hco/22/GRCh38#17810992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929572-C-A

17811009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929584-G-A

http://identifiers.org/hco/22/GRCh38#17811033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929606-C-A

17811048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929622-C-G

17811048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929622-C-T

http://identifiers.org/hco/22/GRCh38#17811058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929632-A-C

http://identifiers.org/hco/22/GRCh38#17811181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120929757-C-A

17811181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929757-C-G

17811181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929757-C-T

17811280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929863-G-T

17811316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120929906-G-T

17811420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930017-C-T

http://identifiers.org/hco/22/GRCh38#17811430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120930027-A-C

17811435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930032-A-G

17811436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930033-T-A

17811436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930033-T-C

17811436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930033-T-G

17811437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930034-T-G

17811460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930047-T-C

17811491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120930074-T-C

17811553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930137-G-A

17812223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930344-T-C

17812225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930346-C-G

17812372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930472-G-C

17812372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930472-G-T

17812421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930508-T-C

http://identifiers.org/hco/22/GRCh38#17812486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120930574-C-A

17812486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120930574-C-T

http://identifiers.org/hco/22/GRCh38#17812724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120930799-C-A

17812724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930799-C-T

17812752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930813-C-G

17812763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930824-G-A

17812763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930824-G-T

17812878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930918-T-A

17812878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930918-T-G

http://identifiers.org/hco/22/GRCh38#17812884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120930924-C-A

17812884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120930924-C-T

http://identifiers.org/hco/22/GRCh38#17812951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120930970-C-A

http://identifiers.org/hco/22/GRCh38#17813204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931140-C-A

17813204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931140-C-G

17813204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931140-C-T

http://identifiers.org/hco/22/GRCh38#17813212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931150-C-A

17813212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931150-C-T

17813308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931252-G-T

http://identifiers.org/hco/22/GRCh38#17813474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931359-C-A

http://identifiers.org/hco/22/GRCh38#17813745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931654-C-A

17813745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931654-C-T

17813770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931655-T-A

17813770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931655-T-C

17813782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931667-G-A

http://identifiers.org/hco/22/GRCh38#17813794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931679-C-A

17813818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931703-A-G

http://identifiers.org/hco/22/GRCh38#17813830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120931715-C-A

17813830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931715-C-T

17813854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931739-T-C

17813876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931765-G-T

17813885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931771-G-T

17813935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120931806-G-T

17815092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933209-T-C

17815112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933229-G-C

17815112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933229-G-T

http://identifiers.org/hco/22/GRCh38#17815128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120933246-C-A

17815128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933246-C-T

http://identifiers.org/hco/22/GRCh38#17815135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120933253-C-A

17815135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933253-C-T

17815141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933259-A-G

http://identifiers.org/hco/22/GRCh38#17815159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120933274-A-C

17815173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933288-G-A

17815208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933332-T-C

17815240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933371-T-C

17815266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933393-T-C

17815294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933419-T-C

17815309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933438-G-A

17815309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933438-G-T

http://identifiers.org/hco/22/GRCh38#17815331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120933458-C-A

17815331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933458-C-T

17815365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933497-A-G

17815382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933517-C-T

http://identifiers.org/hco/22/GRCh38#17815448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120933591-C-A

17815448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933591-C-G

17815569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933715-T-C

17815580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933726-G-A

17815615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120933761-G-T

17815730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933869-C-T

17815731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933870-G-A

17815731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933870-G-C

17815731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933870-G-T

17815746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933890-G-C

17815799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933945-C-T

17815826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120933992-T-G

17815880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934059-C-T

17816567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934534-T-G

17816572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934539-G-A

17816572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934539-G-T

http://identifiers.org/hco/22/GRCh38#17816622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120934598-C-A

17816622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934598-C-G

17816626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934602-C-T

http://identifiers.org/hco/22/GRCh38#17816637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120934607-C-A

17816637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934607-C-T

http://identifiers.org/hco/22/GRCh38#17816771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120934741-C-A

17816814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934785-A-G

17816859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934810-T-C

17816859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934810-T-G

17816862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934814-G-A

17816862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934814-G-T

17816959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120934876-T-G

http://identifiers.org/hco/22/GRCh38#17817011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120934931-C-A

http://identifiers.org/hco/22/GRCh38#17817022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120934942-A-C

17817223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120935121-T-G

http://identifiers.org/hco/22/GRCh38#17817277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935169-C-A

17817277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120935169-C-T

http://identifiers.org/hco/22/GRCh38#17817299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935192-C-A

17817299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120935192-C-T

http://identifiers.org/hco/22/GRCh38#17817330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935221-C-A

17817330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935221-C-T

17817384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935275-G-A

17817393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935284-G-A

http://identifiers.org/hco/22/GRCh38#17817402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935293-C-A

17817402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935293-C-T

17817437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935328-A-G

17817552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935443-G-A

17817558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935449-T-C

17817692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935583-C-T

17817720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935611-A-G

17817750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935641-T-C

http://identifiers.org/hco/22/GRCh38#17817763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935645-C-A

17817763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935645-C-T

http://identifiers.org/hco/22/GRCh38#17817939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120935814-C-A

17817939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935814-C-T

17817953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935829-C-G

17817953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935829-C-T

17818046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935910-G-T

17818089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935953-A-G

17818113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120935977-G-A

17818113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935977-G-C

17818113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120935977-G-T

17818183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120936047-G-T

17818272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936142-T-G

17818278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936148-T-G

http://identifiers.org/hco/22/GRCh38#17818284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120936154-C-A

17818284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936154-C-G

17818284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936154-C-T

17818296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936166-G-C

17818296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936166-G-T

17818356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936226-G-T

17818437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936307-G-A

17818437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936307-G-T

http://identifiers.org/hco/22/GRCh38#17818488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120936358-C-A

17818488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936358-C-G

17818488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936358-C-T

17818791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936661-G-A

http://identifiers.org/hco/22/GRCh38#17818830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120936700-C-A

17818830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936700-C-T

17818869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936739-G-C

http://identifiers.org/hco/22/GRCh38#17818959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120936838-C-A

17818959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120936838-C-G

17818959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120936838-C-T

17819161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937030-A-G

17819164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937033-T-C

17819185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937054-G-A

17819185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937054-G-T

17819215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937080-G-A

17819215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937080-G-T

http://identifiers.org/hco/22/GRCh38#17819217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120937082-C-A

17819217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937082-C-G

http://identifiers.org/hco/22/GRCh38#17819274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120937134-C-A

17819274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937134-C-T

http://identifiers.org/hco/22/GRCh38#17819282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120937142-A-C

17819317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937177-T-G

17819347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937200-G-C

17819500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937352-G-A

17819546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937400-T-C

17821273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937826-G-C

17821362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937898-A-G

17821399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937935-T-C

17821424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120937950-T-C

17821445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120937971-G-C

17821445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120937971-G-T

17821459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120937985-G-C

17821459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120937985-G-T

17821507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 120938033-G-A

17821507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 120938033-G-C

http://identifiers.org/hco/22/GRCh38#17821637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120938147-C-A

17821637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120938147-C-T

http://identifiers.org/hco/22/GRCh38#17821899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120938431-C-A

17821899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120938431-C-T

17821972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120938497-T-G

17822027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120938541-C-T

17822050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120938564-G-A

17822050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 120938564-G-C

17822055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120938569-G-A

17822055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120938569-G-T

17822076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120938593-C-T

17822079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120938596-C-T

http://identifiers.org/hco/22/GRCh38#17822189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120938713-A-C

17822860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939620-C-T

17822928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939691-G-A

17822928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939691-G-T

17822931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939698-G-A

17822931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939698-G-C

17822932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939699-A-G

17822991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120939757-G-A

17822994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120939760-G-A

http://identifiers.org/hco/22/GRCh38#17823114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120939876-C-A

17823114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939876-C-T

http://identifiers.org/hco/22/GRCh38#17823192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120939936-C-A

17823192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120939936-C-T

17824110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940644-T-G

17824369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940820-G-C

17824369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940820-G-T

17824388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940843-T-A

17824523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940954-G-A

17824557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120940998-T-A

17824600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941278-T-C

17824722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941409-T-A

17824722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941409-T-C

17824750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941437-G-A

17824820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941502-G-A

http://identifiers.org/hco/22/GRCh38#17825060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120941748-C-A

17825319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120941977-A-G

17825387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942031-G-A

17825484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942113-G-A

17825484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942113-G-C

17825656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942312-C-T

http://identifiers.org/hco/22/GRCh38#17825714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120942359-A-C

17825742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942370-G-A

17825762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942387-A-G

17825816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942439-C-G

17826068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942628-T-C

17826121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942678-C-T

17826231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942789-C-T

17826366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942921-G-A

17826366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942921-G-T

17826420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942977-G-A

17826420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942977-G-T

17826426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942983-G-A

17826426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120942983-G-T

17826492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120943053-T-C

17826558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120943119-T-C

17827201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120945964-G-T

17827244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946000-C-T

17827250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946006-T-C

http://identifiers.org/hco/22/GRCh38#17827275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946026-A-C

17827423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946154-T-C

17827442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946173-C-T

http://identifiers.org/hco/22/GRCh38#17827573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946243-C-A

17827573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946243-C-T

http://identifiers.org/hco/22/GRCh38#17827574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946244-C-A

17827574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946244-C-G

17827574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946244-C-T

17827636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 120946308-G-A

17827636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 120946308-G-C

17827636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 120946308-G-T

http://identifiers.org/hco/22/GRCh38#17827668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946340-C-A

17827668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120946340-C-T

17827705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 120946377-A-G

http://identifiers.org/hco/22/GRCh38#17827743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946415-C-A

17827743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120946415-C-T

17827780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 120946452-G-A

17827780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 120946452-G-C

17827780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 120946452-G-T

17827819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946491-G-A

17827819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946491-G-C

17827819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946491-G-T

17827833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946508-G-A

17827833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946508-G-C

17827833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946508-G-T

http://identifiers.org/hco/22/GRCh38#17827872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120946561-C-A

17827903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946592-A-G

17827930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946627-T-A

17827930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946627-T-C

17827952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946651-C-T

17827995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946712-C-T

17828045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946759-G-A

17828045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946759-G-T

17828137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946855-C-T

17828320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946979-C-T

17828321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946980-G-A

17828329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120946988-G-C

17828357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947015-T-C

17828369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947027-C-T

17828389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947046-T-C

17828395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947052-T-C

17828475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947143-G-A

17828534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947194-G-A

17828534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947194-G-C

17828617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947283-G-A

17828876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120947618-G-C

17829923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120948576-G-A

17829966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120948615-T-C

17830203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120948852-C-T

17830315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949003-T-C

http://identifiers.org/hco/22/GRCh38#17830415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120949045-A-C

17831062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949517-G-C

17831168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949624-T-A

17831229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949678-C-G

17831397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949797-C-T

17831399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120949799-C-T

17831811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120950316-T-C

17831906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120950416-A-G

http://identifiers.org/hco/22/GRCh38#17831915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120950425-C-A

17831915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120950425-C-T

http://identifiers.org/hco/22/GRCh38#17831918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120950428-C-A

17831918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120950428-C-T

17832065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120950566-C-T

http://identifiers.org/hco/22/GRCh38#17832083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120950584-C-A

17832083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120950584-C-T

17832112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 120950613-G-A

http://identifiers.org/hco/22/GRCh38#17832180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120950670-C-A

17832240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120950713-G-A

17832240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120950713-G-C

17832240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120950713-G-T

17832257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120950730-A-T

17834750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120953967-C-T

17834830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954023-C-T

17834831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954024-A-G

17835029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954174-C-T

17835081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954224-G-T

17835105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954250-T-A

17835393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954517-C-G

17835483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954607-C-T

17835576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954785-C-T

17835646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120954853-C-T

http://identifiers.org/hco/22/GRCh38#17837097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120955653-A-C

17837226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120955746-G-A

17837251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120955770-T-C

17837259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120955778-T-G

17837286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120955801-C-G

17838655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957234-C-T

17838660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957239-A-G

17838733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957306-A-G

http://identifiers.org/hco/22/GRCh38#17838750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120957323-C-A

17838756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957329-C-T

17838757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957330-G-A

17838835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120957553-C-T

17840280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957724-C-G

17840290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957734-T-C

17840298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957742-G-A

17840298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957742-G-C

17840298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957742-G-T

http://identifiers.org/hco/22/GRCh38#17840299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120957743-C-A

17840299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957743-C-T

http://identifiers.org/hco/22/GRCh38#17840318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120957777-C-A

17840318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957777-C-G

17840360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957823-G-A

17840360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120957823-G-T

http://identifiers.org/hco/22/GRCh38#17840387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120957846-C-A

17840628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958044-A-G

http://identifiers.org/hco/22/GRCh38#17840680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120958095-C-A

17840680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958095-C-T

17840710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958108-T-A

17840719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958117-A-G

17840768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958139-T-C

17840805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958175-T-C

17840876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958235-A-G

17840884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958243-T-C

17840894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958253-A-G

17840901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958260-G-T

17840904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958263-T-G

17840905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958264-G-A

17840945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958288-C-T

http://identifiers.org/hco/22/GRCh38#17840978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120958320-C-A

17840978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120958320-C-T

http://identifiers.org/hco/22/GRCh38#17841859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120959530-C-A

17841859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120959530-C-G

17841859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120959530-C-T

17843267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120960565-G-C

17843384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120960679-G-A

17843415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120960704-G-A

17843739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120961399-T-C

17844751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962301-C-T

17844957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962478-C-T

17844962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962483-C-G

17844962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962483-C-T

17845000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962516-C-T

17845027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962540-A-G

17845334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962782-C-T

17845338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962786-G-A

17845400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962846-A-G

17845475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120962898-G-A

17845664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963057-T-C

http://identifiers.org/hco/22/GRCh38#17845692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120963085-A-C

17845692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963085-A-G

17845755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963144-C-T

17845888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963251-T-C

17846090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963432-C-T

17846152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120963497-G-A

17846363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964140-C-G

17846363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964140-C-T

17846368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964145-C-G

http://identifiers.org/hco/22/GRCh38#17846622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120964379-C-A

17846622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964379-C-T

17846623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964380-G-A

17846740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964630-T-C

17846980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964869-G-A

17846986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964873-C-G

17847063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964949-G-A

17847063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120964949-G-C

17847159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120965017-C-G

17847159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120965017-C-T

17847201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120965037-C-T

17848137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966232-C-G

17848156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966250-G-A

17848212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966315-C-G

17848483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966540-C-T

17848488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966747-T-C

17848634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966915-G-C

17848654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966937-G-C

17848654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120966937-G-T

17849480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120967908-G-A

17849688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120968050-A-G

17849688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120968050-A-T

17849719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120968064-G-A

17850905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120968894-T-C

17855045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120969446-G-A

17855070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120969472-C-T

http://identifiers.org/hco/22/GRCh38#17855209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120969620-C-A

17855254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120969728-C-T

17857662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120972250-G-A

17857725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120972314-G-A

17857811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120972372-T-G

17857980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120972518-G-A

17857981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120972519-G-T

17858549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973006-G-A

17858549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973006-G-C

17858549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973006-G-T

http://identifiers.org/hco/22/GRCh38#17858965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120973372-C-A

17858965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973372-C-T

17859058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973443-G-C

17859208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973472-G-A

17859621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120973794-T-A

17859906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974019-C-T

17859935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974050-G-C

17860019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974128-T-A

17860019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974128-T-C

http://identifiers.org/hco/22/GRCh38#17860078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120974191-C-A

17860078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974191-C-T

17860080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974193-C-T

http://identifiers.org/hco/22/GRCh38#17860092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120974205-C-A

17860092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974205-C-G

http://identifiers.org/hco/22/GRCh38#17860097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120974210-C-A

17860097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120974210-C-T

http://identifiers.org/hco/22/GRCh38#17860407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120974574-C-A

http://identifiers.org/hco/22/GRCh38#17860468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120974634-C-A

17860468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120974634-C-T

17860488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120974653-G-T

17860663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120974820-G-A

17860871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975042-G-A

17860991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975142-A-T

17861087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975251-T-C

17861099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975263-A-G

17861185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975363-G-T

17861204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975385-G-A

17861224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975402-G-A

17861224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975402-G-T

17861401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975553-C-T

http://identifiers.org/hco/22/GRCh38#17861470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120975599-C-A

17861470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975599-C-T

17861550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975661-G-A

17861550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975661-G-T

17861578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975683-T-A

17861625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975738-C-G

17861629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975742-T-C

17861747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975860-T-A

17861809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975921-A-G

http://identifiers.org/hco/22/GRCh38#17861813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120975924-C-A

17861813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975924-C-T

17861823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975933-T-A

17861831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975941-G-A

17861832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975942-C-G

17861832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120975942-C-T

17861935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976056-G-A

17861935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976056-G-C

http://identifiers.org/hco/22/GRCh38#17861954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976075-C-A

17861999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976118-G-T

http://identifiers.org/hco/22/GRCh38#17862574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976301-C-A

http://identifiers.org/hco/22/GRCh38#17862701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976425-C-A

17862720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976453-G-T

http://identifiers.org/hco/22/GRCh38#17862740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976475-C-A

17862769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976493-G-C

17862817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976536-C-T

17862855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976561-G-A

http://identifiers.org/hco/22/GRCh38#17862909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976613-C-A

17862909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976613-C-T

17862981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976650-C-T

http://identifiers.org/hco/22/GRCh38#17863073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976735-C-A

17863073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976735-C-G

17863129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976790-A-G

http://identifiers.org/hco/22/GRCh38#17863194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120976848-C-A

17863194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976848-C-T

17863252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120976883-T-C

17863457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977041-G-T

http://identifiers.org/hco/22/GRCh38#17863497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977061-C-A

17863497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977061-C-T

17863513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977076-T-C

17863619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977182-T-C

17863650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977211-G-A

17863650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977211-G-T

http://identifiers.org/hco/22/GRCh38#17863653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977214-C-A

http://identifiers.org/hco/22/GRCh38#17863682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977243-C-A

17863690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977254-C-G

17863690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977254-C-T

http://identifiers.org/hco/22/GRCh38#17863700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977274-C-A

17863807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977360-A-T

17863899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977455-G-A

17863899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977455-G-T

http://identifiers.org/hco/22/GRCh38#17863939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977683-C-A

17863940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977684-A-G

17863940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977684-A-T

http://identifiers.org/hco/22/GRCh38#17863955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120977700-C-A

17863977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977718-G-T

17864025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977763-T-C

17864029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977767-T-C

17864089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977813-T-C

17864089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977813-T-G

17864095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977818-T-A

17864095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977818-T-C

17864095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120977818-T-G

http://identifiers.org/hco/22/GRCh38#17864358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120978063-C-A

17864360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978065-G-A

17864360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978065-G-T

17864383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978071-G-A

17864383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978071-G-C

http://identifiers.org/hco/22/GRCh38#17864393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120978081-C-A

17864471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978155-G-T

http://identifiers.org/hco/22/GRCh38#17864508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120978204-C-A

17864508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978204-C-T

17864518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978212-G-A

17864518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978212-G-C

17864518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978212-G-T

17864555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978244-G-A

17864555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978244-G-T

17864569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978256-G-A

17864569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978256-G-T

17864653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120978323-A-G

17864744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 120978414-C-T

17864912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120978582-A-G

17865040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120978706-C-T

17865269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120979025-G-C

17866042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979866-C-G

17866042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979866-C-T

http://identifiers.org/hco/22/GRCh38#17866091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120979917-C-A

17866091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979917-C-T

http://identifiers.org/hco/22/GRCh38#17866112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120979938-C-A

17866112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979938-C-T

http://identifiers.org/hco/22/GRCh38#17866119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120979940-C-A

17866119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979940-C-T

17866137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120979957-T-A

17866399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120980186-C-G

17866399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120980186-C-T

17866746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120980731-T-C

17866843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120980838-G-A

http://identifiers.org/hco/22/GRCh38#17868029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120983280-A-C

17868096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120983338-G-A

17868495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120983860-C-T

17870545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120984926-T-C

17870830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985188-T-A

17870979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985330-T-C

http://identifiers.org/hco/22/GRCh38#17871199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120985525-C-A

17871199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985525-C-T

17871386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985655-T-C

17871536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985725-G-T

17871673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985803-A-G

17871744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985868-T-G

http://identifiers.org/hco/22/GRCh38#17871767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120985886-C-A

17871767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985886-C-T

http://identifiers.org/hco/22/GRCh38#17871769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120985888-C-A

17871769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985888-C-T

17871788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985907-C-T

http://identifiers.org/hco/22/GRCh38#17871805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120985925-C-A

17871834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120985953-C-T

17872018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120986137-G-A

17872018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120986137-G-T

17872030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120986149-G-A

17872030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120986149-G-T

17872032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986151-G-A

17872032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986151-G-T

17872085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986189-T-C

17872104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986212-G-A

17872104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986212-G-C

17872104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986212-G-T

http://identifiers.org/hco/22/GRCh38#17872113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120986221-C-A

17872113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986221-C-T

http://identifiers.org/hco/22/GRCh38#17872142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120986241-C-A

17872142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986241-C-T

17872227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986339-G-A

17872269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986385-T-C

17872279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986395-G-A

http://identifiers.org/hco/22/GRCh38#17872641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120986630-C-A

17872641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986630-C-G

17872641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986630-C-T

http://identifiers.org/hco/22/GRCh38#17872686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120986678-C-A

17872686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986678-C-G

17872686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986678-C-T

17872689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986681-G-A

17872696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986688-T-G

17872700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986692-A-T

17872702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986694-G-A

17872702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986694-G-T

17872722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986714-C-T

http://identifiers.org/hco/22/GRCh38#17872737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120986728-C-A

17872737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986728-C-G

17872737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986728-C-T

17872964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120986955-T-C

17873030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120987020-A-G

17873057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120987051-G-T

17873924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120987962-C-G

17874090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120988139-G-T

17874209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120988259-G-A

17874284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120988365-G-A

17874376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120988600-C-T

http://identifiers.org/hco/22/GRCh38#17874726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120988922-A-C

17875082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989117-T-C

http://identifiers.org/hco/22/GRCh38#17875192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120989212-C-A

17875192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989212-C-T

17875198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989218-C-T

17875217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120989237-G-A

17875217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120989237-G-T

17875237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120989254-A-T

http://identifiers.org/hco/22/GRCh38#17875316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120989311-C-A

17875316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120989311-C-T

17875320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120989315-T-A

http://identifiers.org/hco/22/GRCh38#17875330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120989316-C-A

17875330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120989316-C-T

http://identifiers.org/hco/22/GRCh38#17875342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120989328-C-A

17875572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989553-G-A

17875572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989553-G-C

17875572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989553-G-T

17875633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989608-T-C

17875633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989608-T-G

17875718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989676-A-G

17875796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989750-G-A

17875892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989831-C-T

17875932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120989855-T-C

17876070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120990026-C-T

17876146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120990103-T-C

17876259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120990216-G-A

17876259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120990216-G-T

17876309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120990250-A-G

17876436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120990343-G-T

17876439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120990347-G-A

17876439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120990347-G-T

17876462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120990370-C-G

17876550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120990437-G-T

http://identifiers.org/hco/22/GRCh38#17878240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120990837-C-A

17878320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120990889-C-T

17878422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120990961-C-T

http://identifiers.org/hco/22/GRCh38#17878423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120990962-C-A

17878515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991027-C-T

17878752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991233-C-T

17878845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991323-C-T

17879174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991624-T-C

17879214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991662-T-C

17879217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991665-G-A

17879217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991665-G-T

17879244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991690-G-A

17879253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991699-G-A

17879253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991699-G-T

17879321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991766-A-G

17879392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120991835-T-A

17879392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120991835-T-C

17879452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991881-G-A

17879511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991942-G-A

17879511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120991942-G-T

http://identifiers.org/hco/22/GRCh38#17879525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120991956-A-C

17879669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992079-G-C

17879760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992162-T-C

17879893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992278-A-G

17879893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992278-A-T

17879936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992328-G-A

17880119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992476-C-T

17880168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992521-C-G

17880201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992551-G-A

17880201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992551-G-T

17880278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992613-G-T

17880344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992673-T-A

17880378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992807-C-T

17880397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992879-G-A

17880441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992922-C-T

17880442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992923-G-A

17880442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992923-G-T

17880509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120992994-T-C

17880923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993423-G-A

17880969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993455-G-A

17881027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993512-G-C

17881027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993512-G-T

17881246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120993763-G-A

17881366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993883-G-T

17881395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993918-G-A

17881395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993918-G-C

17881406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993929-G-A

17881406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993929-G-T

17881407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993930-G-C

17881407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993930-G-T

17881410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993933-G-A

17881410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993933-G-T

http://identifiers.org/hco/22/GRCh38#17881434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120993956-C-A

17881434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120993956-C-T

17881569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120994098-T-A

17881609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120994137-G-A

17882116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120994575-T-A

17882116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120994575-T-C

17882447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120994887-C-T

17882658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120995047-T-G

17883308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120995739-T-G

17884007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996413-C-T

17884236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996619-G-A

17884236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996619-G-T

17884237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996620-A-G

http://identifiers.org/hco/22/GRCh38#17884318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120996700-A-C

17884327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 120996709-G-T

17884482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996864-G-A

17884482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996864-G-T

http://identifiers.org/hco/22/GRCh38#17884502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120996890-C-A

17884502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996890-C-G

17884502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120996890-C-T

17884604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997002-T-C

17884767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997127-G-A

17884815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997165-T-A

17885171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997422-T-C

17885228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997472-C-T

17885276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120997518-G-C

http://identifiers.org/hco/22/GRCh38#17885556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120997784-A-C

http://identifiers.org/hco/22/GRCh38#17885768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120998071-C-A

17885768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120998071-C-T

http://identifiers.org/hco/22/GRCh38#17885804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120998082-A-C

17885849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120998122-G-A

http://identifiers.org/hco/22/GRCh38#17885986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120998252-C-A

17885986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120998252-C-T

http://identifiers.org/hco/22/GRCh38#17886016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120998282-C-A

17886016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120998282-C-T

http://identifiers.org/hco/22/GRCh38#17887273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120999286-A-C

17887329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120999351-A-G

17887476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999495-G-A

17887476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999495-G-C

17887520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999539-G-C

17887520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999539-G-T

17887527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999551-G-A

17887527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999551-G-T

17887680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999676-A-G

17887929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120999901-T-G

17888773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001430-T-C

17888786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001443-C-T

17888787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001444-G-A

17889005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121001575-G-A

17889005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121001575-G-T

http://identifiers.org/hco/22/GRCh38#17889113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121001679-C-A

17889113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121001679-C-G

17889113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121001679-C-T

17889152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121001718-G-A

http://identifiers.org/hco/22/GRCh38#17889239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121001805-C-A

17889239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001805-C-G

17889253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001823-C-T

17889264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001834-A-G

http://identifiers.org/hco/22/GRCh38#17889307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121001876-C-A

17889307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001876-C-T

http://identifiers.org/hco/22/GRCh38#17889342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121001910-C-A

17889342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001910-C-G

17889342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001910-C-T

17889345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121001913-T-C

17890588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003138-C-T

17890653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003203-A-G

17891195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003717-G-A

17891384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003839-T-C

17891392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003847-A-G

http://identifiers.org/hco/22/GRCh38#17891397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121003852-A-C

17891397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121003852-A-T

http://identifiers.org/hco/22/GRCh38#17891730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121004158-C-A

17891730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004158-C-T

17891731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004159-T-G

17892130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004569-C-T

17892234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004652-T-C

17892237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004655-T-C

17892587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004925-G-T

17892631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121004967-C-T

17892746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005070-C-T

17892809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005132-C-T

17892831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005157-C-T

17892968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005291-T-C

17892990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005324-G-A

17893030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005385-C-T

17893138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005493-G-A

17893216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005544-C-T

http://identifiers.org/hco/22/GRCh38#17893234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121005558-C-A

17893234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121005558-C-T

17893570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006383-C-G

17893608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006422-A-G

17893682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006512-T-G

17893742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006556-A-G

17893768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006582-G-A

17893768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006582-G-T

17893838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006638-A-T

http://identifiers.org/hco/22/GRCh38#17893844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121006644-C-A

17893844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006644-C-T

17893847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006647-G-C

17893847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006647-G-T

17893863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121006663-G-A

17893863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006663-G-C

17893863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121006663-G-T

17894020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006882-A-T

17894067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006932-G-T

17894140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121006994-G-A

17894170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007019-G-A

17894170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007019-G-T

17894383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007186-A-G

17895043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007715-A-G

17895116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007743-G-A

17895234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007884-A-T

17895275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121007948-A-G

17895368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121008042-A-G

17895468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121008132-T-G

17895503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121008163-C-G

17895505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121008165-T-C

17895530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121008194-T-C

17895790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010200-G-A

17895826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010236-G-A

17895900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010301-T-C

17895955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010356-T-A

http://identifiers.org/hco/22/GRCh38#17896104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121010538-C-A

17896104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010538-C-T

17896164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010597-G-A

17896164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010597-G-T

17896344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121010757-T-C

17896609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121010880-G-T

http://identifiers.org/hco/22/GRCh38#17896632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121010881-C-A

17896669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010915-T-C

17896669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010915-T-G

17896708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010973-C-T

17896710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121010975-T-C

17896769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 121011036-G-A

17897004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011268-G-A

17897004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011268-G-C

17897009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011273-G-A

17897009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011273-G-T

17897046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011319-C-T

http://identifiers.org/hco/22/GRCh38#17897053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121011326-C-A

17897053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011326-C-T

17897062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011335-A-G

http://identifiers.org/hco/22/GRCh38#17897076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121011347-C-A

17897076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011347-C-G

17897076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011347-C-T

17897081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011351-A-G

17897081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011351-A-T

http://identifiers.org/hco/22/GRCh38#17897187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121011404-C-A

17897297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011420-C-T

17897606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011559-T-C

17897669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011637-T-A

17897837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121011797-C-T

http://identifiers.org/hco/22/GRCh38#17898102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121012018-C-A

17898102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012018-C-T

17898154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012057-T-C

17898241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012142-G-A

17898241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012142-G-C

17898358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012235-G-T

http://identifiers.org/hco/22/GRCh38#17898407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121012283-C-A

17898410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012286-G-A

17898601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121012472-T-C

http://identifiers.org/hco/22/GRCh38#17899058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121013026-C-A

17899104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013072-C-T

http://identifiers.org/hco/22/GRCh38#17899190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121013163-C-A

17899190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013163-C-T

17899432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013418-G-A

17899432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013418-G-T

17899585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013575-C-T

17899678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013652-C-T

17899761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013731-T-A

17900011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121013944-G-C

17900626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014243-G-A

17900661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014273-G-A

17900663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014275-G-A

17900709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014313-A-G

17900709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014313-A-T

17900742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014346-A-G

http://identifiers.org/hco/22/GRCh38#17900757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121014361-C-A

17900757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014361-C-T

http://identifiers.org/hco/22/GRCh38#17900769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121014373-C-A

17900769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014373-C-T

17900906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121014469-T-C

17900930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121014493-A-G

17900951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121014514-C-T

17901069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014593-G-A

17901069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014593-G-T

17901077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014601-T-A

17901077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014601-T-C

17901086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014610-C-T

17901088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014612-G-A

17901094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014618-G-T

17901784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014899-G-C

17901784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014899-G-T

17901836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014923-T-C

17901844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014931-G-A

17901844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014931-G-T

http://identifiers.org/hco/22/GRCh38#17901857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121014944-C-A

17901857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014944-C-G

17901857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014944-C-T

17901869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121014956-G-T

17902002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015092-T-C

17902005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015095-G-A

17902005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015095-G-T

http://identifiers.org/hco/22/GRCh38#17902009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121015099-C-A

17902009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015099-C-T

http://identifiers.org/hco/22/GRCh38#17902010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121015100-A-C

17902095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015163-G-A

17902095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015163-G-T

http://identifiers.org/hco/22/GRCh38#17902543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121015361-C-A

17902680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121015497-A-G

17902725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121015542-T-C

17902784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015601-T-C

17902795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015612-G-A

17902795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015612-G-T

17902805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015619-G-A

17902805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015619-G-T

http://identifiers.org/hco/22/GRCh38#17902809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121015623-C-A

17902809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015623-C-T

17902810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015624-G-A

17902810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015624-G-T

17902819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015636-G-A

17902819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015636-G-T

17902865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015667-C-G

17902872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015674-A-G

http://identifiers.org/hco/22/GRCh38#17902885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121015686-C-A

17903012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015812-G-A

17903087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121015889-T-A

17903255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016013-C-T

17903428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016171-C-G

17903665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016412-A-G

http://identifiers.org/hco/22/GRCh38#17903928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121016678-C-A

17903942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016690-T-C

17904052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016772-C-T

17904129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016810-G-A

17904155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121016832-G-C

http://identifiers.org/hco/22/GRCh38#17904277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121016934-C-A

http://identifiers.org/hco/22/GRCh38#17904523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121017269-A-C

17904591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017308-G-A

17904591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017308-G-C

17904597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017314-G-A

17904597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017314-G-T

17904599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017316-G-A

17904599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017316-G-T

17904666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121017377-A-G

17904831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121017542-G-C

17904855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017566-G-A

17904855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017566-G-T

http://identifiers.org/hco/22/GRCh38#17904865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121017576-C-A

17904865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017576-C-T

17904872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017583-C-T

17904875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017586-T-G

17904876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017587-T-A

17904901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017598-T-C

17904923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017608-C-T

http://identifiers.org/hco/22/GRCh38#17904954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121017624-C-A

17905479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018219-G-T

http://identifiers.org/hco/22/GRCh38#17905628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121018367-C-A

17905643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018380-T-C

17905758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018490-T-C

http://identifiers.org/hco/22/GRCh38#17905992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121018665-C-A

17906123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018794-G-C

17906133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018803-A-G

17906197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018847-C-G

17906231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121018881-G-A

17906426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121017377-A-G

17906819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121019227-T-C

17906910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019325-G-A

17906910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019325-G-C

17906910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019325-G-T

17906950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019357-T-A

17907090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019445-C-T

17907466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019687-C-T

17907688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121019871-G-T

17908004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020158-T-A

17908004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020158-T-C

17908007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020162-C-T

17908653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020427-A-T

17908706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020472-C-T

17908768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020532-G-T

17909126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121020915-G-A

17909296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021064-G-A

17909523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021206-T-C

17909593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021235-G-A

17909593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021235-G-C

17909976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021541-T-C

17910016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021585-G-A

17910084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021645-G-A

http://identifiers.org/hco/22/GRCh38#17910148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121021702-C-A

17910211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121021910-C-T

http://identifiers.org/hco/22/GRCh38#17910258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121021958-A-C

17910514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121022187-C-T

17910532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121022205-C-T

17910758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121022441-C-T

17910820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121022508-C-T

http://identifiers.org/hco/22/GRCh38#17911140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121022823-C-A

17911196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121022881-G-A

17911376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121023031-T-A

17913382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121025871-C-G

17913385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121025875-G-A

17913639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121025986-G-T

17913716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121026083-T-C

17914542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121026775-T-C

17914572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121026799-C-T

17914576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121026803-G-A

17914576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121026803-G-C

http://identifiers.org/hco/22/GRCh38#17914723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121026982-C-A

17914920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027111-T-C

17914941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027132-C-G

17914961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027153-G-A

17915052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027211-G-A

17915079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027238-T-G

17915336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027403-A-T

17915451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027486-G-A

17915452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027487-G-A

17915484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121027516-A-T

http://identifiers.org/hco/22/GRCh38#17916120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121027932-C-A

17916236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028039-C-T

17916237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028040-G-A

17916350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028132-T-C

17916367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028148-G-C

17916407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028177-C-T

17916460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028219-G-A

17916544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121028287-C-T

http://identifiers.org/hco/22/GRCh38#17919551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121029492-A-C

17919551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029492-A-G

17919569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029510-C-T

17919753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029642-C-T

17919842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029696-T-C

17919903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029756-G-A

17919903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029756-G-T

17919934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121029774-C-T

http://identifiers.org/hco/22/GRCh38#17920093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121029918-C-A

17920134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121029957-C-T

17920189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121030011-G-A

17920346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121030180-C-T

17920366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121030598-T-C

17920443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121030675-A-G

http://identifiers.org/hco/22/GRCh38#17920529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121030748-C-A

17921907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031310-C-T

17921959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031351-C-G

17922037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031428-C-T

17922052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031448-T-A

17922052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031448-T-G

http://identifiers.org/hco/22/GRCh38#17922172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121031558-A-C

17922172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031558-A-T

17922232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031584-C-G

17922443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031804-C-T

17922449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031810-T-A

17922624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031929-A-G

17922655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121031958-A-G

17922908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121032235-G-T

17923573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121032784-C-T

17923781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121032951-G-C

17925014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121033866-G-A

17925014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121033866-G-T

17925015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121033867-G-A

17925015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121033867-G-C

http://identifiers.org/hco/22/GRCh38#17925750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121034251-C-A

17926009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121034499-T-A

17926215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121034710-A-G

17926857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121035233-G-A

17926881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121035256-T-C

17927095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121035441-C-T

17931229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037645-T-C

17931284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037714-T-C

17931420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037810-C-T

17931429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037819-C-T

17931505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037889-T-C

17931587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121037966-T-C

17931623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121038005-T-C

17939606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038115-G-A

17939612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038121-C-T

17939779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038271-C-G

17939843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038332-C-T

17940003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038446-G-T

17940266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038680-G-A

17940638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038785-G-A

17940773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038890-G-T

17940842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121038958-G-A

17941074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039112-C-G

17941161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039208-C-T

17941396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039438-A-G

17941427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039466-G-A

17941708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039822-C-T

17941836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039918-G-A

17941890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121039965-G-A

17941963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040050-G-A

17942232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040327-G-T

17942250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040345-C-T

17942439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040538-C-T

17942477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040578-C-T

17942521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040623-G-C

17942584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040649-A-G

17942744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121040761-G-A

17943676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121041434-G-A

17943678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121041436-A-G

17943850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121041580-T-C

17944014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121041765-C-T

17944466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121042125-C-G

17945150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043196-A-G

17945252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043297-C-T

17945270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043315-G-A

17945350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043415-G-A

http://identifiers.org/hco/22/GRCh38#17945516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121043586-C-A

17945637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043706-G-C

http://identifiers.org/hco/22/GRCh38#17945756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121043812-C-A

17945762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043818-C-T

17945896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121043969-C-T

17946013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044076-T-G

http://identifiers.org/hco/22/GRCh38#17946057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121044120-A-C

http://identifiers.org/hco/22/GRCh38#17946230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121044295-A-C

17946303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044359-A-G

17946360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044412-G-C

17946425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044478-C-T

17946426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044479-G-A

17946972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121044977-C-T

17947087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121045086-C-T

17947210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121045184-C-T

17949295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046528-T-G

17949337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046589-G-T

17949389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046642-G-A

17949447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046705-G-A

17949632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046868-T-C

17949643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121046881-G-A

17949844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047071-C-G

17949868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047095-A-G

17949997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047225-A-G

17949997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047225-A-T

17950922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047781-A-G

17951033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121047855-G-A

17951300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121048105-C-T

http://identifiers.org/hco/22/GRCh38#17951501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121048240-C-A

17955776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051571-C-T

17955791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051586-G-C

17955906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051689-G-C

17955976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051750-G-A

17955976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051750-G-T

17956069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051838-G-A

17956069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051838-G-C

17956076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121051845-T-C

17957915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121053624-T-A

17957943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121053650-G-A

17958204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054029-C-T

17958462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054267-C-T

17958505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054292-C-T

17958579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054352-G-A

17958590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054363-G-A

17958643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054413-G-C

17958644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121054414-T-C

17961664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121056364-A-G

17961889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121056530-A-G

17961920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121056552-G-A

17962506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121056892-T-C

17963537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121057874-C-T

17963538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121057875-G-A

17963545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121057882-C-T

17963660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058003-A-T

http://identifiers.org/hco/22/GRCh38#17963663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121058006-C-A

17963670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058010-A-G

17963670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058010-A-T

17963752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058086-G-A

17963854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058177-A-G

17963854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058177-A-T

17963855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058178-T-A

17963855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058178-T-G

17964459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058744-C-G

17964655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121058959-T-C

17969793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062749-C-T

17969906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062637-A-G

17969917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062626-G-A

17969918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062625-G-A

17969969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062585-G-A

17970286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062195-G-A

17970286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062195-G-C

17970341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121062143-G-A

17972134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121063913-T-C

17972312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064111-C-T

17972389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064185-T-C

17972435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064226-T-C

17972495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064279-G-A

17972495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064279-G-C

17972528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064307-G-A

17972550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064329-T-A

17972618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064391-G-A

17972641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064405-A-G

17972746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064522-G-A

17972746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064522-G-T

17972959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064770-C-T

17973122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064916-G-A

17973170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121064965-G-C

http://identifiers.org/hco/22/GRCh38#17973201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121064995-A-C

17974008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121065805-A-G

17974094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121065868-G-A

17974096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121065870-G-A

17975310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067101-A-G

17975497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067631-G-A

17975529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067664-C-T

17975575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067709-C-G

17975677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067803-C-T

17975747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067859-A-G

17975771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067879-T-C

17975788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067896-G-A

17976063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067912-T-A

17976063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121067912-T-G

17976242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068066-C-T

17976274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068093-C-G

17976274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068093-C-T

17976388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068237-A-G

17976441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068301-T-C

http://identifiers.org/hco/22/GRCh38#17976455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121068315-A-C

17976674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121068370-T-C

17983992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121072480-G-A

17984103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121072596-A-G

http://identifiers.org/hco/22/GRCh38#17984207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121072670-C-A

17984536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121072892-C-T

17985112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073322-G-A

17985112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073322-G-C

17985121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073335-G-A

17985155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073381-G-A

17985169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073398-G-A

17985235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073446-C-T

17985369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073574-T-A

http://identifiers.org/hco/22/GRCh38#17985458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121073655-C-A

17985458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073655-C-T

17985485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073681-G-T

17985519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073714-C-T

17985530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073725-G-C

17985797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121073971-C-T

17989691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121077876-C-T

17990307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078519-G-A

17990333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078546-C-T

17990364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078567-T-C

17990491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078671-T-C

17990497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078677-T-C

17990504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078678-T-C

http://identifiers.org/hco/22/GRCh38#17990753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121078923-C-A

17990753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121078923-C-T

17990950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121079111-T-C

17991033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121079190-A-T

17991055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121079202-G-A

17991564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121079762-G-T

17991571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121079769-G-A

http://identifiers.org/hco/22/GRCh38#17991930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121080068-C-A

17992055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121080164-G-A

17992422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121080569-A-G

17992488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121080636-A-T

17993139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121080992-C-G

http://identifiers.org/hco/22/GRCh38#17997000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121083455-A-C

17997543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121083573-T-A

17997587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121083640-C-T

17997764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121083781-A-G

17997785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121083795-G-A

http://identifiers.org/hco/22/GRCh38#17999044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121084169-A-C

17999574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121085353-G-A

18000002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121085718-G-A

18000084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121085788-T-C

18000522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086191-G-A

18000522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086191-G-C

18000595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086272-G-C

18000695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086375-G-A

18000773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086449-G-A

http://identifiers.org/hco/22/GRCh38#18001007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121086626-C-A

18001007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086626-C-T

18001035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121086642-C-T

http://identifiers.org/hco/22/GRCh38#18001093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121086673-C-A

18001093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121086673-C-T

18001097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121086677-G-A

18001097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121086677-G-T

http://identifiers.org/hco/22/GRCh38#18001146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121086745-C-A

18001261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121086870-C-T

18001425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121087008-G-A

18001425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121087008-G-T

18001447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121087045-G-A

18001447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 121087045-G-T

18001546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087153-T-G

18001588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087192-G-T

18001627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121087229-G-A

18001645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087247-G-A

18001645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087247-G-T

http://identifiers.org/hco/22/GRCh38#18001663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121087265-C-A

18001663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121087265-C-G

18001664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087266-T-G

18001707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087309-G-A

18001734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121087336-G-A

http://identifiers.org/hco/22/GRCh38#18003420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121088048-C-A

http://identifiers.org/hco/22/GRCh38#18004120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121088532-C-A

18004120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121088532-C-G

18004120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121088532-C-T

18004125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121088537-A-G

http://identifiers.org/hco/22/GRCh38#18004158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121088571-C-A

18004851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121089653-G-A

18005436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090408-G-A

18005539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090522-G-A

18005539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090522-G-C

http://identifiers.org/hco/22/GRCh38#18005560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121090546-C-A

18005560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090546-C-T

18005673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090569-A-G

18005687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090582-A-G

18005733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090624-G-T

18005750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090641-G-A

18005750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090641-G-T

18005834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090698-T-C

18005835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121090699-G-T

http://identifiers.org/hco/22/GRCh38#18005929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121090772-C-A

18008939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121092383-T-C

18008997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121092443-A-G

18009024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121092471-C-T

18009113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121092558-A-G

18010509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121097713-C-G

18010561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121097761-G-T

18010618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121097839-T-G

18010675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121097864-C-G

18010782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121097971-T-C

18011062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121098343-T-C

18012520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121099646-C-G

http://identifiers.org/hco/22/GRCh38#18012569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121099697-A-C

18012569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121099697-A-G

18012569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121099697-A-T

18012954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121099957-G-A

18013007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121099988-G-A

18013272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121100239-A-T

18013408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121100404-G-A

18013484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121100489-C-T

18013531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121100529-G-A

18013595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121100645-C-T

18014309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121101838-A-G

18014349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121101882-C-G

18017029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104004-G-A

18017030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104005-G-A

18018326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104235-A-G

18018356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104266-C-T

18018369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104279-T-C

18018369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104279-T-G

18021028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121104587-G-C

18021549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105140-A-G

18021560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105151-T-C

18021561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105152-G-C

18021720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105317-T-C

18021742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105340-A-G

18021922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105514-A-G

18021935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105524-T-C

18022012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105605-G-A

18022251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105980-G-A

18022251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121105980-G-T

18022440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106164-T-G

18022688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106254-C-T

18023024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106582-C-T

18023101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106662-T-C

18023493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121106896-T-G

http://identifiers.org/hco/22/GRCh38#18023750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121107183-C-A

18023750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107183-C-G

18024157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107602-T-C

http://identifiers.org/hco/22/GRCh38#18024186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121107627-C-A

http://identifiers.org/hco/22/GRCh38#18024213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121107659-C-A

18024244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107693-G-T

18024260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107709-G-A

18024270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121107719-A-G

18024278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121107727-C-T

18024329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121107779-C-T

18024402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121107847-T-C

http://identifiers.org/hco/22/GRCh38#18024449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121107887-A-C

18024489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24694
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 121107934-G-T