60940959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23682679-T-C

60941522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23682170-T-C

http://identifiers.org/hco/2/GRCh38#60941698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23682007-A-C

60941698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23682007-A-G

60942099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23681652-G-A

60942099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23681652-G-T

60942309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23681438-G-A

http://identifiers.org/hco/2/GRCh38#60942374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23681378-C-A

60942374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23681378-C-T

60942411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23681341-G-A

60942457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23681296-T-A

http://identifiers.org/hco/2/GRCh38#60943022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23681173-C-A

60944923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679159-G-A

60944923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679159-G-T

60944950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679133-G-A

60944950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679133-G-C

60944950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679133-G-T

http://identifiers.org/hco/2/GRCh38#60944981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23679100-A-C

60944981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679100-A-G

60944981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23679100-A-T

60945028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23679053-A-T

60945034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23679047-G-T

60945213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23678881-A-G

60945581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23678254-G-T

60945921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23677620-T-A

60945921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23677620-T-C

60946425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23677216-T-C

60946552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676989-C-T

60946561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676980-T-C

60947051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23676441-A-T

60947454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675932-G-T

60947497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675904-T-A

60947497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675904-T-C

60947721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675733-C-G

60947721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675733-C-T

60948012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675597-G-A

60948012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675597-G-C

60948052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23675563-T-C

http://identifiers.org/hco/2/GRCh38#60948210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23675407-C-A

60948285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23675355-C-T

60948989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23674360-G-A

60949261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23674153-G-A

http://identifiers.org/hco/2/GRCh38#60949663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23673555-A-C

60950660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671980-C-G

60950990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671683-T-C

60951170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23671496-A-G

60952563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670612-A-G

60952834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23670377-C-T

60953004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23670212-T-C

60953052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23670164-A-G

60953762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668977-A-G

60953972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23668763-G-A

60953972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23668763-G-C

60953985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23668750-T-C

60954137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23668595-A-G

60954212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668523-T-A

60954221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668514-G-A

60954221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668514-G-T

60954254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668490-A-G

60954263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668483-G-A

60954263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23668483-G-C

http://identifiers.org/hco/2/GRCh38#60954281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23668465-C-A

http://identifiers.org/hco/2/GRCh38#60954494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23668237-A-C

http://identifiers.org/hco/2/GRCh38#60954551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23668181-A-C

http://identifiers.org/hco/2/GRCh38#60954887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23667708-C-A

60954887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667708-C-T

60954900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667695-A-G

60954980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667654-A-G

60955198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667456-G-A

60955650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667340-T-C

http://identifiers.org/hco/2/GRCh38#60955829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23667169-A-C

60955829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23667169-A-G

60960398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23662317-C-T

http://identifiers.org/hco/2/GRCh38#60960495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23662220-C-A

60960495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23662220-C-G

60960495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23662220-C-T

60960547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23662170-T-C

60960796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661932-G-A

http://identifiers.org/hco/2/GRCh38#60960856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23661767-A-C

60960967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661658-C-T

60961011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661555-A-T

60961195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661383-T-C

60961424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661316-C-G

60961424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23661316-C-T

60961486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23661256-G-A

http://identifiers.org/hco/2/GRCh38#60961654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23661084-C-A

http://identifiers.org/hco/2/GRCh38#60961694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23661044-C-A

60961726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23660335-G-C

http://identifiers.org/hco/2/GRCh38#60961754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23660307-A-C

60961754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23660307-A-G

60962635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23658968-A-G

60962670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23658934-G-C

http://identifiers.org/hco/2/GRCh38#60962677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23658927-C-A

60962677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23658927-C-T

60962812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23658834-A-G

60962826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 23658820-T-G

60962947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23658718-A-G

60965231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23657113-T-C

60965623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656749-A-G

60965623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656749-A-T

60965659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656683-G-A

60965659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656683-G-C

60965659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656683-G-T

http://identifiers.org/hco/2/GRCh38#60965714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23656632-A-C

60965729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23656613-G-C

60965982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23655787-T-C

http://identifiers.org/hco/2/GRCh38#60966036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23655733-C-A

60966523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23655292-C-T

60966599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23655203-A-G

60966838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23654845-T-C

http://identifiers.org/hco/2/GRCh38#60967076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23654624-C-A

60967076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23654624-C-T

60967079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23654621-A-G

60967086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23654615-T-C

60967086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23654615-T-G

http://identifiers.org/hco/2/GRCh38#60967169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23654536-C-A

http://identifiers.org/hco/2/GRCh38#60967248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23653223-C-A

60967248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23653223-C-G

60967248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23653223-C-T

60967274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23653192-G-A

60967577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23652924-A-G

http://identifiers.org/hco/2/GRCh38#60967662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23652850-C-A

60967663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652849-T-C

60967705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652812-T-C

60967733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652784-T-A

60967733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652784-T-G

http://identifiers.org/hco/2/GRCh38#60968262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23652285-C-A

60968262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23652285-C-T

60968995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651480-A-G

60969017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651457-A-G

http://identifiers.org/hco/2/GRCh38#60969019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23651455-A-C

60970264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651278-C-T

60970469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23651047-T-G

60970518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650999-T-A

60970518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650999-T-C

60970603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650921-T-C

60970632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650897-T-C

60970665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650876-A-G

60970845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650677-T-C

60970862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23650653-G-A

60971675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649807-G-A

60971675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649807-G-T

60971677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649805-T-A

60971677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649805-T-C

60971681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649801-G-A

60971681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23649801-G-T

60976778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23648319-G-A

http://identifiers.org/hco/2/GRCh38#60976821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23648277-A-C

60976906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23648188-C-T

60977058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23648030-G-A

http://identifiers.org/hco/2/GRCh38#60977626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23647522-A-C

60977626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23647522-A-G

60977637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23647511-T-C

60977785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23647263-G-C

60977818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23647240-C-T

60978251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646992-A-G

60978317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646941-G-A

60978325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646933-G-A

60978405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646859-G-A

60978409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646855-G-A

60978409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646855-G-C

60978409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646855-G-T

60978505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646720-A-T

60978588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646636-G-A

60978588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646636-G-T

60978880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646386-G-A

60978966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646311-C-T

60979124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23646165-C-T

60979866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23645952-G-A

60984073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23643783-T-A

60984073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23643783-T-C

60984284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23643584-C-T

60984614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23640378-G-C

60984880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23639971-T-C

http://identifiers.org/hco/2/GRCh38#60984985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23639888-C-A

60985059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23639824-T-C

60986144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23639131-A-T

60986511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23638781-T-G

60986732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23638606-G-A

60987172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23637760-A-G

http://identifiers.org/hco/2/GRCh38#60988246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23635323-C-A

60988246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23635323-C-T

60995168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23633240-T-C

60995589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23632858-A-G

60995651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23632797-T-A

60995678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23632770-C-G

http://identifiers.org/hco/2/GRCh38#60995695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23632754-C-A

60995762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23632695-T-C

60996804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23632040-C-G

60997115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23631148-T-G

http://identifiers.org/hco/2/GRCh38#60998001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23630369-C-A

60998001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23630369-C-T

60998246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23630051-T-C

60998547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23629766-G-A

60998598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23629717-G-A

60998625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23629699-G-T

61006517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23623362-T-C

61006517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23623362-T-G

61006561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23623318-C-G

http://identifiers.org/hco/2/GRCh38#61008979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#23622542-C-A

61009230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23622292-C-G

61009324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23622392-T-C

61010662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23619318-A-G

61010662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23619318-A-T

http://identifiers.org/hco/2/GRCh38#61010682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23619298-C-A

61010722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23619258-G-A

61010914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23619065-G-A

61011843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23617334-G-A

61011843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23617334-G-T

61011869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23617308-T-C

http://identifiers.org/hco/2/GRCh38#61011919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23617278-A-C

61011919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23617278-A-G

http://identifiers.org/hco/2/GRCh38#61011966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23617235-C-A

61016796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616700-C-T

61016848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616648-T-C

61016985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616606-A-G

http://identifiers.org/hco/2/GRCh38#61017017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23616572-C-A

61017017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616572-C-T

61017199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616411-G-A

61017272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616338-G-A

61017272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616338-G-C

61017272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616338-G-T

http://identifiers.org/hco/2/GRCh38#61017298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23616312-C-A

61017327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616289-C-G

61017327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616289-C-T

61017333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616283-T-A

61017333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616283-T-C

61017335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616281-G-A

61017335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616281-G-T

http://identifiers.org/hco/2/GRCh38#61017350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23616266-C-A

61017350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616266-C-T

http://identifiers.org/hco/2/GRCh38#61017396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23616218-C-A

61017396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616218-C-T

61017434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616179-T-C

61017435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616178-C-G

61017452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616161-T-C

61017452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616161-T-G

61017456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616157-T-G

61017510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616104-T-C

61017510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23616104-T-G

61017558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616063-G-C

http://identifiers.org/hco/2/GRCh38#61017584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23616010-C-A

61017584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23616010-C-T

61017607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615984-G-A

61017607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615984-G-T

http://identifiers.org/hco/2/GRCh38#61017622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23615976-C-A

61017622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23615976-C-T

http://identifiers.org/hco/2/GRCh38#61017671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23615927-C-A

61017678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615920-T-C

61017678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615920-T-G

http://identifiers.org/hco/2/GRCh38#61017802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23615800-C-A

61017802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615800-C-G

61017802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615800-C-T

61017827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615769-G-A

61017827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615769-G-C

61017827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615769-G-T

61017882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 23615715-T-C

61017953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615645-T-A

61017953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615645-T-C

61018050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23615593-G-A

61018050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23615593-G-C

61018073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615581-C-G

61018088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23615566-G-A

61018088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23615566-G-T

61018130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23615525-C-T

61018205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615448-G-A

61018205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615448-G-C

61018205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26505
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23615448-G-T