41414064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119503254-C-T

41414277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119503472-A-G

41414303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119503483-G-C

41414313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119503493-C-G

41415084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119504246-T-C

http://identifiers.org/hco/15/GRCh38#41415087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119504249-C-A

41415087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119504249-C-T

41415088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119504250-C-T

http://identifiers.org/hco/15/GRCh38#41416991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505429-C-A

41416991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119505429-C-T

http://identifiers.org/hco/15/GRCh38#41417004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505440-A-C

41417004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119505440-A-G

http://identifiers.org/hco/15/GRCh38#41417010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505446-C-A

41417010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119505446-C-G

41417010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119505446-C-T

http://identifiers.org/hco/15/GRCh38#41417201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505649-C-A

41417201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119505649-C-G

41417201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119505649-C-T

41417220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119505668-G-A

http://identifiers.org/hco/15/GRCh38#41417256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505704-C-A

41417256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119505704-C-T

41417319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119505767-G-C

http://identifiers.org/hco/15/GRCh38#41417459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119505893-C-A

41417459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119505893-C-T

41417611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119506047-G-C

41418017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119506416-C-T

41418280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119506667-A-G

41418291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119506678-C-G

41418404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119506779-T-C

http://identifiers.org/hco/15/GRCh38#41419055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119507270-C-A

41419075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119507290-T-C

http://identifiers.org/hco/15/GRCh38#41420149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119508324-A-C

41420333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119508553-C-T

41420762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119509251-T-C

41420786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119509275-A-G

41420970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119509537-A-G

41423175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119510786-A-G

41423223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119510827-G-A

41424370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119511829-C-G

41424380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119511839-G-A

41424386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119511845-G-A

41424386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119511845-G-T

41435536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119520902-T-G

41435658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119521028-A-T

41435899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119521266-G-A

41435962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119521326-A-G

41437587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119521919-A-G

41437785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522068-G-A

http://identifiers.org/hco/15/GRCh38#41438338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119522614-A-C

41438338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119522614-A-G

41438444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522720-G-A

41438451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522727-G-A

41438484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522763-G-A

41438484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522763-G-C

41438484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522763-G-T

41438569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119522834-G-T

41439459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523340-C-G

41440176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523722-G-T

41440907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523863-C-G

41440998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523924-G-T

41443093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525375-A-G

41443171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525988-T-C

41446744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119527011-G-C

41447668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119527662-T-C

41447897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119528089-T-G

41447913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119528104-C-T

41447974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119528159-A-G

41451030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119529914-G-A

41451155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119530004-G-A

41451155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119530004-G-C

41451630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119531212-T-A

41453110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119531766-A-G

41453343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119531890-C-T

http://identifiers.org/hco/15/GRCh38#41457628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119535869-C-A

41457642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119535889-T-C

41457669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119535917-C-T

http://identifiers.org/hco/15/GRCh38#41457691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119535939-C-A

41457691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: synonymous variant
orthologous variants: 119535939-C-T

41457745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: synonymous variant
orthologous variants: 119535993-G-A

41459740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119538322-T-G

41460559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119538804-C-T

41460560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119538805-G-A

41460589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119538850-T-C

41460690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119538957-A-T

41460904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539214-T-G

41461093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539361-A-G

41461372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539654-G-A

41461372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539654-G-C

http://identifiers.org/hco/15/GRCh38#41461382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119539664-A-C

41461382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539664-A-G

41461429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539733-G-A

41461482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539778-G-C

41461514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539855-A-T

41461534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539875-C-T

41461559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539904-C-T

41461598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539931-T-C

http://identifiers.org/hco/15/GRCh38#41461615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119539948-A-C

41461634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539966-C-T

41461638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539970-C-T

41461646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119539978-C-T

41464725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119541396-T-C

http://identifiers.org/hco/15/GRCh38#41465700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119542057-C-A

41465775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542128-G-A

41465853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542165-G-A

41465853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542165-G-T

41466104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542460-G-A

http://identifiers.org/hco/15/GRCh38#41466132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119542481-C-A

41466259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119542608-G-A

41466259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119542608-G-T

41466264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542613-A-G

http://identifiers.org/hco/15/GRCh38#41466300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119542628-C-A

41466300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542628-C-T

41466511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119542825-A-G

41470172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119550552-C-T

41470243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119550633-T-C

41470291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: synonymous variant
orthologous variants: 119550681-C-T

41470360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: synonymous variant
orthologous variants: 119550750-A-G

41470436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119550825-T-G

41471220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: synonymous variant
orthologous variants: 119551604-A-G

41471223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: missense variant
orthologous variants: 119551607-G-T

41471454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119551834-G-T

41471507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119552611-A-G

http://identifiers.org/hco/15/GRCh38#41471547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119552644-A-C

41471701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119552809-C-T

41474394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119555110-G-A

41474426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119555147-G-A

41474441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119555161-T-C

41474542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119555238-G-A

41474565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron variant
orthologous variants: 119555255-G-T

41474597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119555283-G-A

41475455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557131-G-A

41475455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557131-G-C

41475455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557131-G-T

41475516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557189-T-C

41475516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557189-T-G

41475683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557346-A-G

41475694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557357-A-G

41475807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119557469-G-T

41475988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557618-C-T

41476057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557636-G-A

41476075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557654-G-A

41476075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557654-G-C

41476096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557666-G-A

41476163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557733-C-T

41476226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557810-G-T

41476315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557889-G-A

41476315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557889-G-C

41476315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557889-G-T

http://identifiers.org/hco/15/GRCh38#41476319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119557893-C-A

41476319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557893-C-T

http://identifiers.org/hco/15/GRCh38#41476324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119557898-C-A

41476324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557898-C-G

http://identifiers.org/hco/15/GRCh38#41476341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119557915-C-A

41476341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557915-C-T

41476383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557956-C-T

http://identifiers.org/hco/15/GRCh38#41476416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119557989-C-A

41476416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557989-C-G

41476416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119557989-C-T

http://identifiers.org/hco/15/GRCh38#41476543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119558340-C-A

41476543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558340-C-G

41476622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558424-G-A

http://identifiers.org/hco/15/GRCh38#41476636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119558438-C-A

41476636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558438-C-T

41476653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558455-G-A

41476653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558455-G-T

41476733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558516-G-T

41477016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558751-T-G

41477017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558752-G-T

41477052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558789-G-A

41477528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119559233-T-C

41478427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560259-G-A

41478427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560259-G-T

http://identifiers.org/hco/15/GRCh38#41478434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119560266-A-C

41478434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560266-A-G

41478434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560266-A-T

http://identifiers.org/hco/15/GRCh38#41478464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119560299-C-A

41478464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560299-C-G

41478464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560299-C-T

41478574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119560401-A-G

41478756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119560567-G-C

41478756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119560567-G-T

http://identifiers.org/hco/15/GRCh38#41478785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119560597-A-C

41478785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119560597-A-G

41478986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561017-G-A

41478986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561017-G-C

41478986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561017-G-T

41479033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561065-G-T

http://identifiers.org/hco/15/GRCh38#41479301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119561330-C-A

41479301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561330-C-G

41479301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561330-C-T

41479317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561343-G-A

41479318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561344-A-G

41479558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561597-C-T

41480261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119562932-C-G

41480353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119563035-G-T

41480697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563382-G-C

41480697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563382-G-T

41480716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563401-G-A

http://identifiers.org/hco/15/GRCh38#41480724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119563409-C-A

41480724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563409-C-T

41480782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563465-G-A

41480782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563465-G-T

41480905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563575-G-A

41480905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563575-G-C

41480905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563575-G-T

41480906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563576-T-C

41480906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563576-T-G

41481081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563752-G-T

41481163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563833-T-C

41481267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563954-G-A

41481285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563972-G-A

41481285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119563972-G-T

41481358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564061-G-A

41481358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564061-G-T

http://identifiers.org/hco/15/GRCh38#41481596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#119564287-C-A

41481596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564287-C-T

41481597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564288-A-G

41481670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564356-T-C

41481726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564406-G-A

41481738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564422-G-C

41481738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564422-G-T

41481949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564504-G-A

41481949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564504-G-T

41482381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564780-T-C

41482587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119564975-G-T

41482670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119565055-G-A

41482748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119565134-G-A

41483018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119565388-G-T

41483031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119565401-C-T

41483144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119565518-G-A

41483144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119565518-G-T

41483163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119565537-G-A

41483163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119565537-G-T

41483200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28996
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119565572-G-A