115048209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102678404-A-G

115048630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102678033-G-A

115048685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677976-A-G

115048897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677800-T-C

115048915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677780-G-T

115048943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677756-A-G

115049222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677455-A-G

115049320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677352-G-A

115049320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677352-G-T

115049354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102677324-A-T

http://identifiers.org/hco/1/GRCh38#115049765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102676924-C-A

http://identifiers.org/hco/1/GRCh38#115050057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102676633-A-C

115050057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102676633-A-T

http://identifiers.org/hco/1/GRCh38#115050072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102676619-C-A

115050072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102676619-C-T

115050101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102676587-G-T

115050134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3 prime UTR variant
orthologous variants: 102676554-G-T

115050474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102676272-T-C

115050500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102676246-T-C

115050602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102676146-T-C

115050819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675959-C-T

http://identifiers.org/hco/1/GRCh38#115050942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102675845-A-C

115050942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675845-A-G

115051381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675476-C-T

115051656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675238-A-T

115051659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675235-T-A

115051902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102675006-G-T

115052031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102674859-G-C

115052365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102674137-A-G

115052379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102674123-A-G

115052639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102673523-T-C

http://identifiers.org/hco/1/GRCh38#115052976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102672927-C-A

115052976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672927-C-T

115052987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672916-C-T

http://identifiers.org/hco/1/GRCh38#115053386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102672575-C-A

115053386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102672575-C-T

http://identifiers.org/hco/1/GRCh38#115053480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102672478-A-C

115053480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672478-A-G

115053500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672458-T-C

115053500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672458-T-G

115053526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672437-C-G

115053526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672437-C-T

115053597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102672370-T-A

115054210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102671738-C-T

115054310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102671653-T-A

115054590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102671408-T-G

http://identifiers.org/hco/1/GRCh38#115055227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102671069-C-A

115055227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102671069-C-T

115055795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102670475-T-C

http://identifiers.org/hco/1/GRCh38#115056051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102670277-A-C

115056057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102670271-A-G

115056801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669807-C-G

115056860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669753-A-G

115057047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669596-T-G

115057227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669250-A-G

http://identifiers.org/hco/1/GRCh38#115057404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102669067-C-A

115057404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669067-C-G

115057404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102669067-C-T

115057528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102668294-G-A

115057547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102668272-A-G

115057562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102668257-C-T

115057653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102668167-G-A

115057653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102668167-G-T

115057874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667964-T-C

115057905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667942-G-T

115057907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667940-T-A

115057907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667940-T-C

115058129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667717-T-A

115058192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102667692-T-G

http://identifiers.org/hco/1/GRCh38#115058228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#102667659-C-A

115058228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102667659-C-T

115058306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667581-G-C

115058306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667581-G-T

115058378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667514-C-T

115058383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667509-A-T

115058401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667491-G-A

115058401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102667491-G-T

http://identifiers.org/hco/1/GRCh38#115058409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102667483-C-A

http://identifiers.org/hco/1/GRCh38#115058411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102667481-C-A

115058448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667442-G-C

115058448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667442-G-T

115058460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667430-G-A

115058460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667430-G-T

115058477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667412-A-T

115058478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102667411-A-G

115058689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666908-C-G

115058689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666908-C-T

115058693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666904-G-C

115058810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666788-G-T

http://identifiers.org/hco/1/GRCh38#115058989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102666616-A-C

115059291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666521-T-C

115059629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102666235-A-G

115059960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665965-C-T

115060195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665759-T-G

115060311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665696-A-G

115060316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665692-T-G

115060365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665653-T-A

115060365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665653-T-C

115060404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665618-G-A

115060404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665618-G-T

115060422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665604-T-C

http://identifiers.org/hco/1/GRCh38#115060449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102665577-A-C

115060449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665577-A-T

115060474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, missense_variant
orthologous variants: 102665535-C-T

http://identifiers.org/hco/1/GRCh38#115060558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102665454-C-A

115060558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665454-C-G

115060558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665454-C-T

115060559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665453-T-A

http://identifiers.org/hco/1/GRCh38#115061219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102665258-C-A

115061292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102665194-A-G

http://identifiers.org/hco/1/GRCh38#115062026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102664789-C-A

http://identifiers.org/hco/1/GRCh38#115062095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102664738-C-A

115062095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664738-C-G

115062095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664738-C-T

http://identifiers.org/hco/1/GRCh38#115062100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102664733-C-A

115062100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664733-C-T

115062255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664585-G-A

115062255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664585-G-T

115062278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102664546-C-T

http://identifiers.org/hco/1/GRCh38#115062369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102663648-A-C

http://identifiers.org/hco/1/GRCh38#115062494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102663570-C-A

115062494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663570-C-T

115062520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663544-A-G

115062520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663544-A-T

115062673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663399-T-C

115062796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663256-C-T

115062956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663079-C-T

115063019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102663012-C-T

115063171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662874-C-T

115064137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662822-G-A

115064137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662822-G-C

http://identifiers.org/hco/1/GRCh38#115064173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102662788-C-A

115064562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662433-A-G

115064677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662350-C-T

115064734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662296-T-C

115064919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662139-T-A

115065086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662017-T-G

115065096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662007-G-A

115065096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102662007-G-T

115065208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102661900-G-T

http://identifiers.org/hco/1/GRCh38#115065563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102661581-C-A

115065563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102661581-C-T

115067476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102660158-G-T

115067745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659913-G-A

115067745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659913-G-T

http://identifiers.org/hco/1/GRCh38#115067754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102659904-C-A

115067766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659894-G-A

115067889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659793-C-G

115067889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659793-C-T

115067917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659759-A-G

115067917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659759-A-T

115067926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659750-G-A

115067985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659698-C-T

115068050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659632-G-A

http://identifiers.org/hco/1/GRCh38#115068051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102659631-C-A

115068051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659631-C-T

115068204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659476-C-T

115068210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659470-G-C

115068303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659382-C-T

115068399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659292-C-T

115068416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659283-G-A

115068489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659127-T-G

115068553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102659069-T-C

115072370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657570-C-T

http://identifiers.org/hco/1/GRCh38#115072398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102657542-A-C

115072477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657452-G-C

115072493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657436-T-C

115072588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657366-T-G

http://identifiers.org/hco/1/GRCh38#115072788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102657231-C-A

115072788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657231-C-G

http://identifiers.org/hco/1/GRCh38#115072798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102657224-C-A

115072798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657224-C-T

http://identifiers.org/hco/1/GRCh38#115072802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102657220-C-A

115072826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657198-T-C

115073084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102657001-A-G

115073098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron_variant, undefined
orthologous variants: 102656981-G-T

115073140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102656947-A-G

115073633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102656366-T-C

115073640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102656359-A-T

http://identifiers.org/hco/1/GRCh38#115073913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102656066-A-C

115074085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655877-T-G

115074307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655703-T-C

115074310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655700-C-T

115074563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655430-A-G

115074564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655429-A-G

115074564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655429-A-T

115074795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655183-T-C

115074816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655162-G-A

115074928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102655063-C-G

115075465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654542-G-A

115075677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654312-G-A

115075783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654229-C-G

115075783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654229-C-T

115075790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654222-C-T

115075878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102654138-T-C

115076080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653963-G-A

115076083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653962-T-A

115076127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653925-C-T

115076293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653754-A-T

115076348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653697-G-T

115076382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653669-C-T

115076519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653531-G-A

115076611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102653450-C-T

http://identifiers.org/hco/1/GRCh38#115077292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102652907-A-C

115077302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652897-A-T

http://identifiers.org/hco/1/GRCh38#115077359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102652850-C-A

115077482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652750-G-A

115077562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652682-G-A

115078017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652251-T-C

115078026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652241-C-G

115078115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102652158-T-C

115078296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651954-C-G

115078296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651954-C-T

115078344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651909-C-T

115078349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651904-G-C

115078964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651703-A-G

115079214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651505-A-G

115079596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102651121-T-C

115080083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102650511-T-C

115080245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102650328-C-T

115080681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102650205-A-T

115080819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102650089-G-A

115080880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102650028-G-A

115082338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102649008-C-T

115082346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102649000-A-T

115083489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102647524-T-G

115083578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102647448-C-T

115083629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102647391-A-G

115083835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102647213-G-A

http://identifiers.org/hco/1/GRCh38#115083863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102647187-C-A

http://identifiers.org/hco/1/GRCh38#115084111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102646948-A-C

115084145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646914-T-C

http://identifiers.org/hco/1/GRCh38#115084146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102646913-C-A

115084152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646907-T-C

115084684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646380-T-A

115084699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646365-A-G

http://identifiers.org/hco/1/GRCh38#115084724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102646340-A-C

115084776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646292-A-T

115084781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646291-T-C

115084839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646235-C-T

115085074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102646001-C-T

115085473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102645642-T-C

115085824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102645303-C-T

115086685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102644301-T-C

http://identifiers.org/hco/1/GRCh38#115087753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102643902-A-C

115088188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102643505-T-C

115088351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102643347-C-G

115089036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102642659-C-T

115089119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: intron variant
orthologous variants: 102642580-G-C

http://identifiers.org/hco/1/GRCh38#115089454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102642288-C-A

115089454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642288-C-T

http://identifiers.org/hco/1/GRCh38#115089458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#102642284-A-C

115089458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642284-A-G

115089458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642284-A-T

115089501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642243-G-A

115089501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642243-G-C

115089501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20659
most severe consequence: 5 prime UTR variant
orthologous variants: 102642243-G-T