128153492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 88423474-A-G

128153492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 88423474-A-T

128153522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 88423445-G-A

128153522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 88423445-G-T

128153559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 88423408-A-G

128153631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 88423336-A-G

http://identifiers.org/hco/3/GRCh38#128153634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88423333-C-A

128153634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 88423333-C-G

128153634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 88423333-C-T

128153643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 88423324-G-A

128153643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 88423324-G-T

128153853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88423156-T-C

128154106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88422972-A-G

http://identifiers.org/hco/3/GRCh38#128154303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88422820-A-C

128155610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88422167-C-G

128158902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88420964-G-A

128158937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88420923-T-C

128159064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88420809-A-G

128159113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88420761-T-C

128159860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88420177-G-C

128160393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88419579-G-A

128160426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88419547-G-A

128160629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88419339-C-T

http://identifiers.org/hco/3/GRCh38#128160671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88419213-C-A

128160800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418935-A-G

http://identifiers.org/hco/3/GRCh38#128161165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88418555-C-A

128161611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418160-G-A

128161715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88418048-T-C

128161796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88417947-C-T

128162018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88417722-T-C

128162164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88417606-A-G

128162464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88417295-A-G

128163005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88416758-G-C

128163048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88416716-C-T

128164351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414908-C-T

128164361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414899-A-G

128164508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414730-C-T

128164556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414685-G-A

128164556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414685-G-C

128164556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414685-G-T

128164559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414682-G-C

128165304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88414055-A-T

128165465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88413679-C-T

128165581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88413571-C-G

128167029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88412177-C-G

128167084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88412120-G-A

128167129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88412075-C-T

128167673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88411310-T-C

128167828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88411140-A-G

128168363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88410670-A-G

128168710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88410358-G-A

128168917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88410200-A-T

128169576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88409533-C-G

128170035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88409158-T-C

128170827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88408656-A-G

http://identifiers.org/hco/3/GRCh38#128170981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#88408512-C-A

128171051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88408441-T-C

128172867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88407136-A-G

128172904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88407102-A-T

128173208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406828-G-A

128173270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406767-G-T

128173349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406695-G-C

128173405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406650-A-G

128173457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406601-T-C

128173466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406592-C-T

128173571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406486-G-A

128174494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406325-G-A

128174854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406006-G-C

128174860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88406000-A-G

128175230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88405467-T-G

128175375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88405331-G-A

128175397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88405309-G-A

128177794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88403399-C-G

128178089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88403271-A-G

http://identifiers.org/hco/3/GRCh38#128178090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88403270-A-C

128178733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88402780-G-A

128178828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88402693-C-T

128179845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88401803-C-T

128180102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88401577-T-C

128180102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88401577-T-G

128180111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88401569-G-T

128180500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88401075-G-A

128180748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88400946-G-T

http://identifiers.org/hco/3/GRCh38#128181693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88400069-A-C

128181704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88400058-G-A

128183861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88398398-G-A

128183973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88398308-C-T

128184268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88397198-A-G

128184580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88396931-A-G

128187520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88394525-C-T

http://identifiers.org/hco/3/GRCh38#128187521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88394524-A-C

128187742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88394353-C-T

128188207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88393596-T-C

128188293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88393563-G-A

128188602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88393261-A-G

128188875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88393012-C-G

128192628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88391377-A-G

128192820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88391225-T-A

128192831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88391214-G-C

128193312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390799-A-G

128193372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390749-C-G

128193372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390749-C-T

128193670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390453-G-A

128193818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88390319-C-T

128194472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88389800-G-A

http://identifiers.org/hco/3/GRCh38#128195262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88388913-A-C

128195454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88388750-G-A

128195465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88388739-C-T

http://identifiers.org/hco/3/GRCh38#128195613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88388639-C-A

128195613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88388639-C-T

128196736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88387579-G-T

128197042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88387307-A-G

128197652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88387008-C-T

128197832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88386851-T-C

128197917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88386768-A-T

128198382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88386313-T-C

128198571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88386118-T-G

128199448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88385453-C-T

128199606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88385305-T-G

128199632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88385294-G-A

128200121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88385120-G-A

128200654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384896-A-G

128200664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384886-A-G

128200703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384855-A-G

128200801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384763-C-T

128200969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384606-G-A

128200969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88384606-G-T

128204894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381768-G-C

128204935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381728-C-T

128205162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381541-C-T

128205267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88381450-T-A

128205973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380818-C-T

128206028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380764-A-G

128206280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380555-T-C

128206520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380371-A-G

128206612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380331-A-G

128206685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380268-T-G

128206887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380131-G-A

128206975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88380052-C-T

http://identifiers.org/hco/3/GRCh38#128207192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88379873-C-A

128209512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88378714-C-T

128209835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88378439-C-T

128209998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88378280-C-T

128210532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88377887-C-T

128210560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88377859-T-C

128210695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88377733-A-G

128211155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88377364-C-T

128212382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88376719-T-C

128212382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88376719-T-G

128212584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88376555-T-A

128213091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88376199-G-A

128213169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88376150-G-A

128213791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88375644-T-C

128213815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88375573-T-C

128215377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373726-G-A

128215486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373645-T-A

128215486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373645-T-C

128215904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373148-G-A

128215925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373126-G-A

128215956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88373108-A-G

128217427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88372299-C-G

128217721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88372043-C-T

128218474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88371308-G-A

128218642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88371159-A-G

128219477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88370565-G-A

128219634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88370425-C-G

128219733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88370372-T-G

128220237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88369845-C-T

128220342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88369746-C-G

http://identifiers.org/hco/3/GRCh38#128226961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88365658-C-A

128227310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88365305-T-C

128227321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88365294-T-C

http://identifiers.org/hco/3/GRCh38#128227340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88365275-C-A

128227340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88365275-C-T

128227937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88364833-G-T

128229932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363694-C-G

128230879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363349-A-G

128231241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88363110-A-G

128231482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88362778-A-G

128231749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88362553-T-A

128232217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88362148-G-A

128237517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359393-T-C

128237534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88359376-G-A

128237982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358939-A-T

128238406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358526-A-G

http://identifiers.org/hco/3/GRCh38#128238888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88358375-A-C

128238888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358375-A-G

128238935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358321-C-G

128239091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358178-A-G

128239091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88358178-A-T

128243024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88356992-G-A

128243236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88356777-C-T

128243760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88356322-G-A

128244002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88356110-C-G

128244098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88356061-G-A

128244304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88355900-G-C

128244512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88355748-A-T

http://identifiers.org/hco/3/GRCh38#128244633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88355641-A-C

128244986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88355347-A-T

128245130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354942-A-G

128245931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88354252-T-C

128246365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353826-C-T

128246727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353496-T-A

128246727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353496-T-G

http://identifiers.org/hco/3/GRCh38#128246777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88353449-A-C

128246955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88353272-A-G

128247152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353122-A-G

128247329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352881-T-C

128247571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352701-G-A

128248032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352293-A-G

128248954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351396-A-G

128249190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351224-C-T

http://identifiers.org/hco/3/GRCh38#128249377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88351047-A-C

128249377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351047-A-G

128251236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88348503-A-T

128251453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88348316-T-C

128251529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88348274-A-G

128251804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88348008-A-G

128252499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347361-T-C

128252693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347171-A-T

128252751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347115-T-G

128252866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347009-C-G

128253200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88346742-A-G

128255624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345918-A-G

128255745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88344894-T-G

128261494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88336113-G-A

128261583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88336046-G-T

128262036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335712-G-A

128262036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335712-G-T

http://identifiers.org/hco/3/GRCh38#128262280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88335471-C-A

128262289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335462-T-C

128262373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335393-G-T

128262479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335311-A-T

128262539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88335214-C-T

128263444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88333688-A-G

128263608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88333568-C-T

http://identifiers.org/hco/3/GRCh38#128263906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88333127-A-C

128264577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332667-C-T

http://identifiers.org/hco/3/GRCh38#128264801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88332443-C-A

128264801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332443-C-T

128264820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332411-G-A

128264840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332392-G-T

http://identifiers.org/hco/3/GRCh38#128264858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88332374-C-A

128264858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332374-C-T

128264941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332296-G-A

128264998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332234-G-A

128265180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88332084-G-A

128266619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88331247-G-A

128266824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88331105-C-G

128267815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88330231-C-G

128269874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88329431-G-C

128270610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328839-G-A

128270785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328607-G-A

128270806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328587-A-G

128271187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328249-G-C

http://identifiers.org/hco/3/GRCh38#128271237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88328199-C-A

128271329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88328105-A-G

128271723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327617-C-G

128272221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327204-T-A

128272258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327167-C-T

128272316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88327119-T-C

128272929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88326671-C-G

128272929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88326671-C-T

128273171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88326407-G-T

http://identifiers.org/hco/3/GRCh38#128273395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88326207-C-A

128274507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324475-G-C

128274565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324421-A-T

128274566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324420-G-C

128274566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324420-G-T

128274773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324229-C-T

128274827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88324180-G-T

128275069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88323986-T-C

128275394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88323680-C-T

128275867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88323330-G-A

http://identifiers.org/hco/3/GRCh38#128276098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88323179-C-A

http://identifiers.org/hco/3/GRCh38#128276226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88323054-C-A

128276324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88322967-A-G

128276471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88322667-A-G

128276651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88322489-C-T

128276654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88322486-A-G

128276690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88322481-T-C

128277585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321729-G-C

128277654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321665-G-A

128277654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321665-G-T

128277676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321649-C-G

128277676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321649-C-T

128277930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321476-C-T

128278025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321452-T-C

128278493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321206-G-A

128278534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88321150-C-T

128278726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88320984-C-G

128279406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88320390-G-A

128280025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319968-C-T

128280126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319890-A-G

128280157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319875-C-T

128280664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88319450-G-T

128281268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88318914-G-T

128281729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88318470-G-A

128282287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88318076-C-G

128282287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88318076-C-T

128282494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88317874-T-C

http://identifiers.org/hco/3/GRCh38#128282697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88317693-C-A

128282705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88317685-C-T

128282742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88317653-G-A

128283019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88317423-C-G

128283242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88317210-G-T

128283849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88316715-G-A

128284227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88316376-G-C

128284334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88316274-T-A

128285889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315316-C-T

128286022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315188-T-G

128286112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315101-A-G

128286179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88315036-C-T

128286210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312566-G-A

128286313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88312473-C-T

128287610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311173-T-C

128287729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88311090-C-T

128288356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88310104-G-C

http://identifiers.org/hco/3/GRCh38#128294961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88307258-A-C

128295005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88307220-T-C

128295006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88307219-G-A

128295181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88307036-T-G

128296029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88306195-A-G

http://identifiers.org/hco/3/GRCh38#128296268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88305959-C-A

128296497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305760-C-G

128296637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305655-T-G

128296640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305652-C-G

128300862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88305374-C-T

128306749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88299475-C-G

128307365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298873-G-A

128307444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298798-G-T

128309008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298141-G-T

128309088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88298066-A-G

http://identifiers.org/hco/3/GRCh38#128309499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88297659-A-C

128309499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88297659-A-G

128310973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88296435-C-T

128311013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88296402-A-G

128311701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295773-T-C

128312418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295186-G-A

128312418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295186-G-C

128312447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295158-C-G

128312596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88295009-T-C

128313104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294551-G-A

128313416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294240-G-A

128313569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88294107-G-A

http://identifiers.org/hco/3/GRCh38#128314997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88293124-A-C

128315071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293025-G-C

128315082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88293014-A-G

128315134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292959-T-C

128315134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292959-T-G

http://identifiers.org/hco/3/GRCh38#128315205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88292914-A-C

128315321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292800-C-G

128315545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292544-C-G

128315823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88292047-C-T

128316405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88291407-A-G

128316452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88291360-G-C

128316452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88291360-G-T

128316466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88291346-A-G

128316787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88291044-C-T

128318899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88289333-G-T

http://identifiers.org/hco/3/GRCh38#128319028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88289215-A-C

128319167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88289084-T-C

128324934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286274-A-G

128324957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286251-A-T

128325081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88286125-G-A

128325315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285889-G-A

128325979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88285261-G-A

128330598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88283638-G-C

128330641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88283597-C-T

128330682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88283564-C-T

128333272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88281569-T-A

128334464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88280144-C-T

128336489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278969-T-C

128336540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278926-C-G

128336577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278889-G-A

128336577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278889-G-C

128336688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278786-G-A

http://identifiers.org/hco/3/GRCh38#128336856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88278659-C-A

128336925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88278619-G-A

128336925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88278619-G-T

http://identifiers.org/hco/3/GRCh38#128336933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88278611-C-A

http://identifiers.org/hco/3/GRCh38#128336963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88278576-C-A

http://identifiers.org/hco/3/GRCh38#128337236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88278365-C-A

128337236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278365-C-T

128337414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278195-C-G

128337506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88278139-C-T

128337894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88277821-A-T

128337908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88277807-A-G

128338091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88277646-G-A

128338103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88277634-T-C

128338217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88277528-T-A

128339052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88276794-C-T

128339547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88276365-T-C

128340468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88275878-G-A

128340468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88275878-G-T

128340525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88275831-T-G

128341082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88275368-A-G

128341170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88275274-C-G

128341170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88275274-C-T

128341620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88274826-G-A

128341620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88274826-G-C

128341626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88274820-G-A

128341638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88274808-G-T

128341823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: synonymous variant
orthologous variants: 88274623-C-T

128341926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88274527-T-G

128343659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88273551-C-G

128343659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88273551-C-T

128343739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88273492-C-T

http://identifiers.org/hco/3/GRCh38#128343911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88273336-C-A

128343950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88273296-A-G

128346092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88272214-C-T

128346159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88272170-A-G

128346509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88271834-A-G

128347422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88270936-G-C

128349669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88269854-C-T

128350151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88269398-G-A

128350604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88269036-T-C

128350760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88268908-G-A

128350834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88268284-T-A

128351625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88267622-T-C

128351823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88267432-G-T

128351924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88267338-G-A

128353515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88267020-T-C

128353580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266957-C-T

128353652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266889-G-C

128354149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266585-C-T

128354165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266569-G-A

128354191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266549-C-T

http://identifiers.org/hco/3/GRCh38#128354205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88266535-C-A

128354205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266535-C-T

128354277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88266463-G-C

http://identifiers.org/hco/3/GRCh38#128354371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88266336-C-A

128354443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88262829-T-C

128356560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259910-A-T

128356571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259901-T-C

128356875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259678-C-G

128357037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259541-T-C

128357041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259537-T-C

128357156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259423-G-A

128357313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259288-A-G

128357321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259280-A-G

128357461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88259147-G-A

128357747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258970-G-A

128357754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258963-G-A

128358386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258516-A-G

128358512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258482-T-C

128358527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258457-T-C

128358655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258367-C-T

128358810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258253-G-A

128358858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258229-G-A

128358913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88258174-G-T

http://identifiers.org/hco/3/GRCh38#128372557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88255330-C-A

128372655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88255256-T-A

128372742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88255191-C-T

128372799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88255156-C-T

128372839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88255126-C-T

128372922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88255036-C-T

http://identifiers.org/hco/3/GRCh38#128373405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88254651-A-C

http://identifiers.org/hco/3/GRCh38#128373541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88254556-C-A

128373553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88254544-C-T

http://identifiers.org/hco/3/GRCh38#128373640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88254483-A-C

128373657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88254465-C-G

128378246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88252891-A-G

128378396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88252793-G-A

128379161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88252170-C-T

128379846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88251542-A-G

128379936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88251466-A-G

128380040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88251364-C-T

128380362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88251115-C-G

128380362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88251115-C-T

128380881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88250331-C-T

128382435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88249408-G-A

128382435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88249408-G-T

128382841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88249112-C-T

128382961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88249020-C-G

128383051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88248952-C-T

128383291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88248760-A-G

128389574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88246250-C-G

128397744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88241764-T-C

128397776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88241738-A-G

128399394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88240418-G-A

128399604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88240201-G-C

128399604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88240201-G-T

128399891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88240022-G-A

http://identifiers.org/hco/3/GRCh38#128400004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88239926-A-C

http://identifiers.org/hco/3/GRCh38#128400777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88239432-C-A

128400777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88239432-C-G

128401010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88239222-C-G

128401034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88239198-C-T

128401162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88239107-G-C

128401250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88239028-A-G

128402343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88238823-T-G

128403944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88237336-T-G

128403982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88237300-A-G

128404119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88237189-T-C

128404620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88236772-C-T

128404925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88236549-G-A

128404931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88236543-C-T

128405331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88236449-G-A

http://identifiers.org/hco/3/GRCh38#128407994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88235444-A-C

128408167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 88235273-G-A

128408167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 88235273-G-T

http://identifiers.org/hco/3/GRCh38#128408328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88235130-A-C

http://identifiers.org/hco/3/GRCh38#128408489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88234980-C-A

128408489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234980-C-T

128408591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234893-G-A

128408591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234893-G-T

128408610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234875-G-A

128408610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234875-G-C

128408610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88234875-G-T

128408700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234823-T-G

http://identifiers.org/hco/3/GRCh38#128408702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88234821-C-A

128408702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234821-C-G

128408708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234817-G-A

128408708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234817-G-T

128408709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234816-G-A

http://identifiers.org/hco/3/GRCh38#128408738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#88234787-C-A

128408738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88234787-C-T

128409572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron_variant, undefined
orthologous variants: 88234076-G-T

128410687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88233363-C-T

128410891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88233184-G-A

128410902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88233170-G-C

128410906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24614
most severe consequence: intron variant
orthologous variants: 88233166-C-T