206651650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662039-G-A

206651650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662039-G-T

http://identifiers.org/hco/2/GRCh38#206651652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63662041-A-C

206651652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662041-A-G

206651670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662059-T-C

206651670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662059-T-G

206651674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662063-G-T

206651742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662131-G-T

206651765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63662156-G-T

http://identifiers.org/hco/2/GRCh38#206651973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63662359-C-A

206652038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63662430-G-A

206652038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63662430-G-T

206652303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63662636-A-G

206652371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63662709-C-T

206652834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63663567-A-G

206653037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63663721-G-A

206653069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63663753-G-T

http://identifiers.org/hco/2/GRCh38#206659002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63667744-C-A

206659002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63667744-C-T

206659146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63667885-G-A

206659146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63667885-G-T

206659188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63667930-T-G

206659821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63668608-T-C

206660561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63671065-T-C

http://identifiers.org/hco/2/GRCh38#206660586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63671090-C-A

206661047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63671426-C-T

206662689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63672240-C-T

206663071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 63672745-G-A

http://identifiers.org/hco/2/GRCh38#206663114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63672776-C-A

206663114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63672776-C-T

206663148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672810-G-A

http://identifiers.org/hco/2/GRCh38#206663197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#63672859-C-A

206663197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672859-C-G

206663250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672912-G-A

206663250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672912-G-T

206663252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672914-T-A

206663310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63672972-G-A

206663374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63673036-G-A

206663384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63673046-C-T

206663410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673077-C-T

206663460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673120-A-G

206663460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673120-A-T

206663526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673190-C-T

http://identifiers.org/hco/2/GRCh38#206663707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63673378-A-C

206663863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673526-C-T

206663920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63673568-G-A

http://identifiers.org/hco/2/GRCh38#206665601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63679960-A-C

206665746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680072-T-C

206665755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680081-A-G

206665756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680082-A-G

206665787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680114-G-A

206665787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680114-G-T

206665820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680165-G-C

206665839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680184-C-T

206667345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680760-G-A

206667357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63680772-T-C

206667924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63681250-G-A

206668171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63681469-G-A

206670274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63682238-C-T

http://identifiers.org/hco/2/GRCh38#206670469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63682417-C-A

206670516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63682487-T-A

206670516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63682487-T-C

206670617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63682588-T-C

206670905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63682933-T-A

206670964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63682986-C-T

206671008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63683029-G-A

206671008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63683029-G-T

206672371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63684217-G-A

206677385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63685078-A-T

206679027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686567-A-G

http://identifiers.org/hco/2/GRCh38#206679037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63686577-C-A

206679037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686577-C-T

206679038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686578-T-C

http://identifiers.org/hco/2/GRCh38#206679053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63686590-C-A

206679053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686590-C-T

http://identifiers.org/hco/2/GRCh38#206679109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63686631-C-A

206679109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686631-C-T

http://identifiers.org/hco/2/GRCh38#206679129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63686651-C-A

206679129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686651-C-T

206679161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63686683-A-G

http://identifiers.org/hco/2/GRCh38#206679405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63687162-C-A

206679548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63687289-T-C

206679694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63687448-A-G

206679948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63687649-A-G

206693168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63698022-C-T

206693259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63698110-C-T

206693285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63698136-G-A

206693358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63698408-G-A

http://identifiers.org/hco/2/GRCh38#206693651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63698705-A-C

206693702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63698756-A-G

206693739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63698791-C-T

206693805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63698848-C-T

206693900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63698943-T-C

206693982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699044-A-G

206694019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699086-G-A

206694117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699180-G-A

206694148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699246-T-A

206694151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699249-G-A

206694208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699297-A-G

206694336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699428-G-A

206694346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699438-G-A

206694359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699451-C-T

206694548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63699635-T-A

206694696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63700223-G-T

206694698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63700225-T-A

206694698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63700225-T-C

http://identifiers.org/hco/2/GRCh38#206694721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63700248-C-A

206694721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63700248-C-T

206694841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63700373-G-A

206694841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 63700373-G-T

http://identifiers.org/hco/2/GRCh38#206694872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63700404-C-A

206694872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63700404-C-T

206694873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63700405-G-A

206694873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63700405-G-T

http://identifiers.org/hco/2/GRCh38#206694943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63700470-A-C

206694943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700470-A-G

206694960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700487-G-A

206694960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700487-G-T

206696988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700530-T-G

206697122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700673-G-A

206697216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63700742-T-C

http://identifiers.org/hco/2/GRCh38#206697859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63701551-C-A

206698095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63701774-T-C

206698132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63701809-T-C

206698149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63701828-A-G

206698219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63701886-T-C

http://identifiers.org/hco/2/GRCh38#206698261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63701929-A-C

http://identifiers.org/hco/2/GRCh38#206698283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63701951-C-A

206698302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63701970-A-G

206698340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63702008-T-C

206698485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63702150-G-A

206698485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63702150-G-T

206698500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63702187-T-C

206699038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703007-C-T

206699576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703413-G-C

206699576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703413-G-T

http://identifiers.org/hco/2/GRCh38#206699588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63703424-C-A

206699619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703452-A-G

206699664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703497-G-A

http://identifiers.org/hco/2/GRCh38#206699668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63703501-C-A

206699668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703501-C-T

206699721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703553-C-T

206700042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703858-T-C

206700105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703894-T-A

206700105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703894-T-C

206700128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63703917-A-G

206700178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63703965-A-G

206700184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63703971-C-T

206700211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63703998-T-A

206700262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704048-T-C

206700334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704111-G-A

206700334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704111-G-T

206700337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704114-G-A

206700337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704114-G-T

206700405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704185-A-T

206700407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704187-T-C

206700440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704210-G-A

206700537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704309-T-A

206700537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704309-T-C

206701223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704792-A-G

http://identifiers.org/hco/2/GRCh38#206701227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63704797-C-A

206701466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63704983-A-T

206701742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63705273-T-C

206701742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63705273-T-G

206702119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706315-G-A

http://identifiers.org/hco/2/GRCh38#206702177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63706373-C-A

206702177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706373-C-T

206702201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706397-G-A

206702201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706397-G-T

206702535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706719-A-G

206702580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63706804-C-G

206702918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707139-G-A

206702978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707200-G-A

206702999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707221-A-G

206703231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707480-G-A

http://identifiers.org/hco/2/GRCh38#206703254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63707503-C-A

206703313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707563-C-T

206703358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707606-T-C

206703368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707616-G-A

206703369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63707617-A-T

206704906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63714078-G-T

206704953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714125-T-C

206704955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714130-G-A

http://identifiers.org/hco/2/GRCh38#206704964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63714139-A-C

206704964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714139-A-G

206705565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714403-T-A

206705624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714462-T-C

206705665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714490-T-A

206705733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714843-T-G

206705738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63714848-G-T

206705915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715029-G-A

206705935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715047-G-T

206705953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715065-T-A

206705974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715086-T-C

206706030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715138-G-A

206706205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715310-G-A

http://identifiers.org/hco/2/GRCh38#206706266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63715360-C-A

206706266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715360-C-T

206706290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715372-C-T

206706440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715527-A-G

206706457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715547-G-A

206706480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715570-G-T

206706518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715600-G-T

http://identifiers.org/hco/2/GRCh38#206706564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63715645-C-A

206706564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715645-C-T

206706600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715656-T-C

206706622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715678-A-T

206706785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715798-A-G

206706785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715798-A-T

206706950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63715940-G-A

http://identifiers.org/hco/2/GRCh38#206707167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63716137-A-C

206707276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63716250-T-A

206707296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63716270-C-G

206707296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63716270-C-T

206707368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63716342-T-C

206707384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 63716358-T-A

206707429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63716403-G-A

206707429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63716403-G-C

206707456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63716430-T-C

206707734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63716661-A-G

206708452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717373-T-A

206708452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717373-T-C

206708519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717440-T-A

http://identifiers.org/hco/2/GRCh38#206708561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63717481-A-C

206708587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717523-A-G

206710317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717730-C-T

206710350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717762-C-T

206710351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717763-G-A

206710351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717763-G-T

206710390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717807-G-A

206710390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717807-G-T

http://identifiers.org/hco/2/GRCh38#206710414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63717831-C-A

206710415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717832-C-T

206710424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717841-G-T

206710445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717862-G-A

206710445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717862-G-T

http://identifiers.org/hco/2/GRCh38#206710496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63717913-C-A

206710496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63717913-C-T

206710707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63718118-G-A

206710707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63718118-G-T

http://identifiers.org/hco/2/GRCh38#206711954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63718257-A-C

206712027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63718330-A-G

206712027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63718330-A-T

http://identifiers.org/hco/2/GRCh38#206713165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63719780-C-A

206713299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63719920-T-C

206713597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720179-T-A

206713639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720589-C-G

206713639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720589-C-T

206713813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720788-T-C

206713932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720903-G-A

206713932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63720903-G-C

206714047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63721019-A-G

206714174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63721156-T-A

206716548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63722687-T-C

206716951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63723071-T-A

206717112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63723194-G-A

http://identifiers.org/hco/2/GRCh38#206717133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63723215-A-C

206717366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63723429-G-A

206717366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63723429-G-C

206718166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63724172-T-A

206718293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724293-T-C

206718298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724303-T-C

206718310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724315-A-G

206718327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724332-A-G

206718368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724370-G-A

206718368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724370-G-T

206718375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724377-G-A

206718375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63724377-G-T

206718399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: 63724393-A-G

206718399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: 63724393-A-T

http://identifiers.org/hco/2/GRCh38#206718402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63724395-C-A

206718417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724409-G-A

206718417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724409-G-C

206718417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724409-G-T

206718418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724410-T-A

206718418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724410-T-G

206718419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724411-G-A

206718419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63724411-G-T

http://identifiers.org/hco/2/GRCh38#206718428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63724421-C-A

206718465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63724460-G-A

206718465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63724460-G-T

http://identifiers.org/hco/2/GRCh38#206718521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63724499-A-C

206718723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63724691-G-T

206721288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63725811-G-A

206721374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63725893-G-C

206721431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: 63725951-C-T

206721435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: 63725955-C-G

206721435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23279
most severe consequence: non coding transcript exon variant
orthologous variants: 63725955-C-T