http://identifiers.org/hco/5/GRCh38#95646832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76166760-C-A

95646843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166749-G-A

95646843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166749-G-T

95646857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166735-G-T

http://identifiers.org/hco/5/GRCh38#95646900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76166667-C-A

95646900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76166667-C-T

95646940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166641-G-A

95646950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76166631-T-C

http://identifiers.org/hco/5/GRCh38#95647015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76166579-C-A

95647015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166579-C-T

95647091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76166524-T-C

http://identifiers.org/hco/5/GRCh38#95647178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76166457-C-A

95647178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76166457-C-G

95647200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166427-T-C

95647327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166325-C-T

http://identifiers.org/hco/5/GRCh38#95647406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76166250-C-A

95647406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166250-C-T

95647498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166208-C-T

95647709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166017-T-C

95647720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76166011-G-A

95647750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76165980-A-G

95647750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76165980-A-T

95647765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76165965-G-C

95647854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76165838-A-G

http://identifiers.org/hco/5/GRCh38#95647871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76165821-A-C

http://identifiers.org/hco/5/GRCh38#95647944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76165770-C-A

95647944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76165770-C-G

95648106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165608-C-G

95648106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165608-C-T

95648156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165594-C-T

http://identifiers.org/hco/5/GRCh38#95648172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76165578-C-A

95648196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165554-T-G

95648230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165517-A-T

95648245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165502-C-T

95648619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162890-T-C

95648875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162640-A-T

95648934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162609-A-G

95648934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162609-A-T

95648954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162601-G-T

95648969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162586-A-T

95648993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162562-T-C

95649279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162188-A-G

95649414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76162031-A-G

95649448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76161998-T-C

95649591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76161893-A-G

95649840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76161662-T-G

95650608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76160273-T-C

95651831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76159047-G-A

95651899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158979-G-T

95651910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158968-G-T

95651989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158902-T-C

http://identifiers.org/hco/5/GRCh38#95652013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76158879-C-A

95652056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158842-A-G

http://identifiers.org/hco/5/GRCh38#95652118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76158812-C-A

95652118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158812-C-T

95652225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76158715-T-C

95653936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76156579-A-G

95653948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76156566-T-G

95654401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76156066-A-G

95654569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76155885-T-G

95655417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76152073-T-C

http://identifiers.org/hco/5/GRCh38#95655418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76152072-C-A

http://identifiers.org/hco/5/GRCh38#95655460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76152034-C-A

95655460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76152034-C-T

http://identifiers.org/hco/5/GRCh38#95655480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76152014-C-A

95655481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76152013-A-T

95655492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76152009-C-T

95655523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151929-G-T

95655567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151895-G-A

95655567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151895-G-C

95655567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151895-G-T

95655630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151849-A-G

95655630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151849-A-T

95655875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151629-G-C

95655875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151629-G-T

95655876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151628-A-T

http://identifiers.org/hco/5/GRCh38#95655992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76151261-C-A

95656058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151193-C-G

95656058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 76151193-C-T

95656229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 76151022-A-G

95656370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150869-T-C

95656387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150855-T-C

95656387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150855-T-G

95656405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150835-T-C

95656433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150595-A-G

http://identifiers.org/hco/5/GRCh38#95656455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76150573-C-A

95656492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150535-A-G

95656852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150118-A-G

95656940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150017-A-T

95656949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76150007-T-C

95656950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 76150006-A-G

http://identifiers.org/hco/5/GRCh38#95657034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76149760-C-A

95657153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149645-G-T

95657194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149611-G-A

95657201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149604-G-A

95657331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149475-A-G

95657584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149276-G-T

95657630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149201-C-T

http://identifiers.org/hco/5/GRCh38#95658015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76148790-C-A

95658150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76148512-T-C

http://identifiers.org/hco/5/GRCh38#95658159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76148503-C-A

95658213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76148449-C-T

95658371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76147799-A-G

95658482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76147028-T-A

95658482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76147028-T-C

95658517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146993-A-G

95658517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146993-A-T

http://identifiers.org/hco/5/GRCh38#95658518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76146992-A-C

95658518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146992-A-G

95658519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146991-G-A

95658519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146991-G-T

95658551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146966-A-T

http://identifiers.org/hco/5/GRCh38#95658598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76146920-A-C

95658630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146885-T-C

95658660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146855-A-G

95658788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146724-C-G

95658788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 76146724-C-T

95658987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146521-T-C

95659013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146498-C-G

http://identifiers.org/hco/5/GRCh38#95659043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76146466-C-A

95659043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146466-C-T

http://identifiers.org/hco/5/GRCh38#95659049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76146460-C-A

95659049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146460-C-T

95659515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76146332-T-C

95659634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 76146234-A-G

95664046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 76141133-G-T

95664050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 76141129-T-A

95664050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 76141129-T-C

95664064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76141115-A-G

95664064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76141115-A-T

95664065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76141114-G-T

95664284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76140988-T-G

95664792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76140500-G-C

95666461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76139618-A-T

95666465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76139614-A-G

http://identifiers.org/hco/5/GRCh38#95666541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76139551-A-C

95667160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138941-A-G

95667318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138787-G-A

95667318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138787-G-C

95667318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138787-G-T

95667322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138783-G-A

95667322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138783-G-C

95667381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138744-C-T

95667502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138559-C-G

95667552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138497-T-C

95667590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138460-G-T

95667711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138351-T-C

95667768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76138280-T-G

http://identifiers.org/hco/5/GRCh38#95668429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76137704-A-C

http://identifiers.org/hco/5/GRCh38#95669148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76137021-A-C

95669156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76137013-G-A

95669296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136882-G-A

95669297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136881-G-A

95669945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136254-G-C

95670083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136116-G-A

95670083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136116-G-T

http://identifiers.org/hco/5/GRCh38#95670179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76136037-C-A

95670179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76136037-C-T

95670596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135608-T-C

95670599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135605-T-C

95670600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135604-T-C

95670703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135489-G-T

95670758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135456-G-A

http://identifiers.org/hco/5/GRCh38#95670846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76135367-C-A

95670846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135367-C-T

95670859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135354-G-A

95670859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135354-G-T

95670881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76135332-C-T

http://identifiers.org/hco/5/GRCh38#95671752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76135096-C-A

95675434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76125872-C-T

95675682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76125602-A-G

95675692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76125592-T-A

http://identifiers.org/hco/5/GRCh38#95679296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76118300-A-C

95679296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76118300-A-G

95679359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76118236-A-G

95679475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76118119-T-G

95679515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76118084-T-C

95680791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76117937-C-T

http://identifiers.org/hco/5/GRCh38#95680821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76117908-C-A

95680821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76117908-C-T

http://identifiers.org/hco/5/GRCh38#95681613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76117081-C-A

95681640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76117054-G-A

95681793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116903-A-G

95681793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116903-A-T

http://identifiers.org/hco/5/GRCh38#95682054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76116724-C-A

95682054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116724-C-T

95682292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116468-T-C

95682461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116321-A-G

95682463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116319-G-A

95682463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116319-G-T

95682498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116286-T-C

95682694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116110-A-T

95682709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116095-G-C

95682709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76116095-G-T

95682896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76115911-A-G

95682966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76115879-A-G

95683082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115756-T-C

95683090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115748-G-A

95683090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115748-G-T

95683161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115677-T-C