http://identifiers.org/hco/15/GRCh38#35169522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114172214-C-A

35169558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114172252-C-T

http://identifiers.org/hco/15/GRCh38#35181691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114179587-C-A

35216051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114212219-T-A

35216283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114213267-A-G

35216456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114213437-G-A

35216959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114214436-C-T

35217092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114214568-G-C

http://identifiers.org/hco/15/GRCh38#35217170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114214648-C-A

35217212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114214687-A-G

35217275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114214749-T-C

35218150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114214932-A-T

35218246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215028-A-T

35218274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215053-A-G

35218275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215054-G-T

35218278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215057-A-G

35218278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215057-A-T

35218340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215120-G-T

35218437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215217-T-A

35218437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215217-T-C

35218734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215504-C-T

35218910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215787-G-A

35218924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114215801-T-C

35219489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114216668-C-G

35219715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114216891-T-A

35219715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114216891-T-G

35219771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114216947-T-C

http://identifiers.org/hco/15/GRCh38#35232694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114225491-C-A

35232694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114225491-C-T

35232816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114225618-C-T

http://identifiers.org/hco/15/GRCh38#35232969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114225827-A-C

35233801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114226316-A-T

35234087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114226634-G-A

35234787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114227449-C-T

35235299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114228079-G-A

35235902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114228612-A-G

35235962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114228668-T-C

35236106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114230469-A-G

35236901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114230881-G-C

http://identifiers.org/hco/15/GRCh38#35237034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114235310-C-A

35237045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235327-T-C

35237045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235327-T-G

http://identifiers.org/hco/15/GRCh38#35238292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114235468-C-A

35238334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235502-T-A

35238334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235502-T-C

35238334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235502-T-G

35238361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235530-C-G

35238361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235530-C-T

35238385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235555-C-T

35238447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235613-T-A

35238447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235613-T-C

35238493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235658-G-A

35238596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235766-C-G

35238596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235766-C-T

35243979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114235924-T-C

35244137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236079-G-T

35244239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236177-G-A

http://identifiers.org/hco/15/GRCh38#35244245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114236183-A-C

35244259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236197-C-T

35244265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236203-T-C

35244405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236333-G-C

35244407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114236335-G-A

35246333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114237596-A-G

35247239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238508-A-G

35247435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238685-A-G

35247453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238702-C-T

35247487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238736-C-T

35247543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238792-T-C

35247609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114238853-G-A

35249019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114239141-T-C

http://identifiers.org/hco/15/GRCh38#35249245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114239331-C-A

35249258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114239344-T-C

http://identifiers.org/hco/15/GRCh38#35249412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114239483-C-A

http://identifiers.org/hco/15/GRCh38#35250665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114240577-C-A

35250665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114240577-C-T

35252712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114241517-G-A

35252950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114241775-A-G

35252950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114241775-A-T

35253025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114241840-C-G

35253266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114242085-A-G

35255294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114243804-C-T

35258224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114247985-G-A

35258224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114247985-G-T

35258263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248023-G-A

35258301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248059-A-T

35258348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248105-T-C

35258385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248143-A-G

35258423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248182-C-T

35258569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248962-C-G

35258598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114248990-T-C

35259354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114251182-C-T

35259547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114251446-G-C

35259557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114251456-T-C

35259612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114251512-T-C

35260931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114252261-C-T

35262155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114253284-T-C

http://identifiers.org/hco/15/GRCh38#35262341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114253640-A-C

35262376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114253674-A-G

35262376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114253674-A-T

35262923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254267-T-A

35263262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254606-C-T

35263330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254673-A-G

35264118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254802-T-A

35264118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254802-T-C

35264137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254813-G-T

35264162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254833-G-A

35264162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114254833-G-T

35264708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114255474-G-A

35264756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114255515-G-A

35264857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114255556-T-G

35265198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114255880-T-C

http://identifiers.org/hco/15/GRCh38#35265383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114256007-C-A

35265478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114256099-T-C

35265521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114256140-A-G

35265633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114256394-C-T

35265926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114256852-T-C

35265953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114256883-T-C

35266142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257042-C-G

35266309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257202-T-C

35266336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257228-T-C

35266487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257385-C-T

35266665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257559-G-A

35266683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114257577-T-C

35267201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114258079-G-A

35267490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114258337-C-G

35267490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114258337-C-T

35267507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114258359-C-T

35267534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114258374-G-A

35270201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260026-T-C

35270245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260070-A-G

35270341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260155-C-G

35270341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260155-C-T

35270348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260162-G-A

35271371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260790-T-G

35271468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260875-C-T

http://identifiers.org/hco/15/GRCh38#35271533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114260940-C-A

35271598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114260974-A-G

35271709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261087-T-C

http://identifiers.org/hco/15/GRCh38#35279870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114261391-C-A

35279870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261391-C-G

35279959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261485-T-G

35279976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261503-A-T

35279977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261504-T-C

35280053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261563-G-C

35280216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261797-T-A

35280216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114261797-T-C

35280659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262038-G-A

35280719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262103-G-C

35281128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262607-A-G

http://identifiers.org/hco/15/GRCh38#35281266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114262741-A-C

35281305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262780-G-A

35281332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262812-T-C

35281338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262818-C-T

35281470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114262949-T-C

35283645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114265643-G-A

http://identifiers.org/hco/15/GRCh38#35283648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114265646-C-A

35283662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114265660-T-C

35283757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114265752-T-C

35284576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266303-T-C

35284768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266489-T-C

35285141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266547-A-G

35285216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266627-T-C

35285253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266660-A-G

http://identifiers.org/hco/15/GRCh38#35285702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114266952-C-A

35285702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114266952-C-T

35285954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267188-T-C

35286201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267438-G-T

35286211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267448-G-T

35286340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267574-G-A

http://identifiers.org/hco/15/GRCh38#35286349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114267583-C-A

35286365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267599-G-C

http://identifiers.org/hco/15/GRCh38#35286417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114267652-C-A

35286503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114267737-C-G

http://identifiers.org/hco/15/GRCh38#35286638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114267866-A-C

35287124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114268330-T-C

35287281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114268504-C-T

35287494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114268709-G-T

35287793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114269006-G-A

35288426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114269579-G-T

35288754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114269902-A-G

http://identifiers.org/hco/15/GRCh38#35288946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#114270080-C-A

35288946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114270080-C-T

35289561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114270698-T-C

35289811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114270953-C-T

35290083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114271227-G-T

35290086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114271230-A-G

http://identifiers.org/hco/15/GRCh38#35290102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114271246-C-A

http://identifiers.org/hco/15/GRCh38#35290536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114271686-A-C

35290540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114271690-C-T

http://identifiers.org/hco/15/GRCh38#35290711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114271861-C-A

35290736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114271885-C-G

35290736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114271885-C-T

35290865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272006-A-T

35290929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272067-A-G

35291069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272204-C-T

35291201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272336-C-T

35291297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272068-A-G

35291298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272067-T-C

35291486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272402-C-T

35291880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272804-C-G

35291921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272845-T-C

35291991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114272911-T-C

35292112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273021-T-C

35292141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273047-C-T

35292450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273322-T-C

35292886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273749-T-G

http://identifiers.org/hco/15/GRCh38#35292941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114273807-C-A

35293006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273872-G-A

35293097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114273961-T-G

35293982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114274812-T-C

35294168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114275006-T-C

http://identifiers.org/hco/15/GRCh38#35294601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114275869-C-A

35294628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114275897-C-T

35294635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114275904-C-G

35294661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114275930-G-A

35294703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114275970-C-G

35294834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114276097-G-A

35294834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114276097-G-C

http://identifiers.org/hco/15/GRCh38#35295153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114276370-A-C

35295153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114276370-A-G

35295399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114276581-T-G

35295426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114276621-C-T

35300569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114279248-G-C

35300579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114279257-G-A

35300579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114279257-G-C

35300630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114279314-T-C

35300838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114279514-C-T

35302929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114281394-T-C

35302982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114281457-T-C

35303062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114281534-T-C

35303667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114282720-A-G

35303879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283182-T-A

35304119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283387-G-A

http://identifiers.org/hco/15/GRCh38#35304214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114283587-A-C

35304214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283587-A-G

35304286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283663-G-A

35304307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283685-A-G

35304364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283733-T-G

35304387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114283756-G-C

http://identifiers.org/hco/15/GRCh38#35304499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114283868-C-A

35304685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114284055-G-T

http://identifiers.org/hco/15/GRCh38#35304808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114284259-A-C

35304808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114284259-A-G

35305412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114284841-C-T

35305545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114284980-T-G

35305550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114284985-T-G

35305684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114285229-T-C

35305728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114285273-T-C

35305850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114285417-C-T

35305866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114285433-G-A

35306310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114285868-G-A

35307600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286321-T-C

35307661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286370-T-G

35307725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286420-T-A

35307793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286485-A-G

35307968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286624-C-T

35308231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114286914-T-A

35308534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114287306-T-C

35308724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114287481-T-C

35308846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114287597-G-T

35309283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114288003-A-G

35310004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114288870-T-G

35310027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114288888-G-A

35310058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114288919-C-T

35310185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289056-T-C

35310279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289148-G-A

35310304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289173-C-T

35310393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289252-G-A

35310518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289373-C-T

35310532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289386-T-C

35310924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289690-T-G

35311197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114289959-T-C

35311507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114290435-T-C

35311578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114290499-G-A

35311986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114290898-A-G

35311988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114290900-T-A

35311988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114290900-T-G

35312578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114291304-T-C

35322780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317012-T-C

35322942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317190-G-A

35322949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317199-T-A

35323081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317338-C-T

35323112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317369-T-C

35323179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317416-T-C

35323671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114317904-G-T

35323940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114318149-A-G

35323949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114318158-G-A

35323991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114318196-T-C

http://identifiers.org/hco/15/GRCh38#35325287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114318846-A-C

35325388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114318963-G-A

35325445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319017-G-A

35325491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319052-A-G

35325613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319102-A-G

35325613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319102-A-T

35326162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319608-T-C

35326170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319616-A-G

http://identifiers.org/hco/15/GRCh38#35326251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114319741-C-A

35326494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114319911-C-T

35327018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114320197-G-T

35327692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114320551-C-T

35328030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114320897-T-C

35328258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321450-G-T

35328276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321468-T-C

35328276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321468-T-G

35328396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321591-C-T

35328410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321605-G-C

35328429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321623-G-A

35328429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114321623-G-T

35329643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114322497-C-G

35330017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114322874-T-C

35330017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114322874-T-G

35330266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114323126-G-A

35330442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114323302-G-C

35330442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114323302-G-T

35330820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114323660-T-C

35330842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114323682-G-A

http://identifiers.org/hco/15/GRCh38#35331015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114323833-C-A

35331112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114323932-A-G

35331196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324018-G-A

35331275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324079-A-G

35331291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324095-G-A

35331378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324163-A-G

35331408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324192-A-G

35331408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324192-A-T

35331473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324250-T-C

35331473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324250-T-G

35331518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324296-T-C

35331912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324675-T-C

35332078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114324816-C-T

35333489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114334790-A-G

http://identifiers.org/hco/15/GRCh38#35333569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114334878-C-A

35333583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114334892-A-G

35333662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114334961-T-C

35342705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335520-G-A

35342705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335520-G-T

35342710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335525-T-A

35342778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335584-A-G

35342807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335609-T-A

35342926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335733-G-A

35342937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114335744-T-C

35343366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114336150-G-C

35343530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337435-T-C

35343580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337477-G-A

35343821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337740-C-G

35343919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337835-G-T

35343998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337907-C-G

35343998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114337907-C-T

35344855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338493-C-T

35345006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338629-T-G

35345018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338641-G-A

35345047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338654-T-A

35345047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338654-T-C

35345072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338679-T-C

35345076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114338683-A-G

35366223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344028-T-C

35366280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344053-C-T

35366436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344170-T-C

35366456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344190-T-G

35366656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344362-C-T

35366720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344420-C-T

35366764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344460-C-T

35366898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344583-T-A

35366898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344583-T-C

35366977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344650-G-A

35367079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344746-T-A

35367079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344746-T-C

http://identifiers.org/hco/15/GRCh38#35367144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114344875-C-A

35367194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114344928-C-T

35367882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114345776-A-G

35368172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346047-G-A

35368172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346047-G-T

35368351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346177-T-C

35368401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346233-C-T

35368407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346239-T-C

35368473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346294-T-C

35370870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114346891-C-T

35370951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114346964-G-A

35371051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347076-T-G

35371267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347309-A-G

35371303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347345-A-G

35371307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347349-A-G

35371420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347568-C-T

http://identifiers.org/hco/15/GRCh38#35371443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114347590-A-C

35371443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347590-A-G

35371443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347590-A-T

35371456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347603-A-T

35371457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347604-G-C

35371457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347604-G-T

35371460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347608-G-A

35371460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347608-G-C

35371460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347608-G-T

35371531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347668-T-G

35371607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347731-T-C

35371659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347780-A-T

35371690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347811-T-C

35371697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347818-T-C

35371699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347820-G-A

35371721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347843-T-C

35371784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347892-A-G

35371857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114347940-T-A

35371998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348636-T-C

35372056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348667-G-A

35372056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348667-G-T

35372069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348687-T-C

35372095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348707-T-C

http://identifiers.org/hco/15/GRCh38#35372097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114348709-C-A

35372097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348709-C-G

35372097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348709-C-T

35372135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348719-G-A

35372135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114348719-G-T

35372156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114348726-A-G

http://identifiers.org/hco/15/GRCh38#35372192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114348762-C-A

35372192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 114348762-C-G

35372192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 114348762-C-T

http://identifiers.org/hco/15/GRCh38#35372235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114348793-A-C

35372235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348793-A-G

35372255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348812-T-C

35372284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114348819-A-G

35372290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114348824-G-T

35372409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348899-G-A

35372409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348899-G-T

35372433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348922-G-T

http://identifiers.org/hco/15/GRCh38#35372444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114348933-C-A

35372444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348933-C-T

35372445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348934-A-G

http://identifiers.org/hco/15/GRCh38#35372463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114348952-A-C

35372500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348988-A-G

35372505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114348993-A-T

35372647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114349127-G-C

35373270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114349823-T-C

35373283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114349841-C-T

35373395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114349982-A-G

http://identifiers.org/hco/15/GRCh38#35373436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114350112-C-A

35373436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350112-C-T

35373438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350114-G-A

35373438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350114-G-T

35373439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350115-T-C

35373485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350158-T-C

35373588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114350260-A-G

35373640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350308-A-G

35373641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350309-T-C

35373656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350324-G-A

35373656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350324-G-T

35373765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350371-A-T

35374084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350622-C-T

35374218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350744-C-G

35374227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114350753-A-G

http://identifiers.org/hco/15/GRCh38#35374301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114350822-A-C

35374467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114351439-C-T

35374502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114351480-G-A

35380320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352103-T-C

35380503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352271-G-T

35380612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352372-T-C

35380714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352465-C-G

35380889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352630-T-C

35381108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114352791-A-T

35381485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353191-T-C

35381552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353258-T-C

35381572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353278-C-G

35381637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353344-C-G

35381696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353403-G-T

35381699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353406-T-A

35381699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353406-T-G

35381733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353440-C-T

http://identifiers.org/hco/15/GRCh38#35381734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114353441-C-A

35381734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353441-C-T

35381754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353461-T-C

35381776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353482-A-G

35381776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353482-A-T

35381810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353513-A-G

35381837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114353540-T-C

35381842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114353545-T-C

http://identifiers.org/hco/15/GRCh38#35381941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114353640-C-A

35381960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353654-T-A

35381960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353654-T-C

35381978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353672-T-A

35382027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114353725-G-T

35383140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114355431-T-C

35383420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114355667-T-C

http://identifiers.org/hco/15/GRCh38#35384245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114356413-C-A

35392028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114360128-T-C

http://identifiers.org/hco/15/GRCh38#35392200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114360273-C-A

35392267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114360336-A-G

35392271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114360340-C-T

35393586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114360760-T-C

35393678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114360855-T-G

35393915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361033-G-C

35394041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361130-C-T

35394160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361219-A-G

35394334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361368-C-T

35394371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361405-T-C

35394958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114361703-T-C

35395348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362054-T-C

35395395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362100-T-C

35395429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362137-T-C

35395475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362183-G-A

http://identifiers.org/hco/15/GRCh38#35395520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114362229-C-A

35395520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362229-C-T

35395565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362271-A-G

35395685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362392-C-T

35395686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362393-A-G

35395835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362562-T-C

35396145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362819-C-T

35396161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114362835-T-G

35409690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114363781-A-T

35409761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114363845-G-C

35410285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365483-T-C

35410285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365483-T-G

35410300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365498-T-C

35410392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365586-T-C

http://identifiers.org/hco/15/GRCh38#35410399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114365593-C-A

35410722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365891-G-A

35410722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365891-G-T

35410731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365900-T-C

35410779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365949-T-C

35410822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114365993-T-C

http://identifiers.org/hco/15/GRCh38#35410960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114366129-C-A

35410960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366129-C-T

35410990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366159-G-A

35410990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366159-G-T

35410993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366162-G-A

35410993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366162-G-C

35410993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366162-G-T

35411018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366187-G-T

35411057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366227-C-G

35411086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114366255-C-T

35416510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114367158-T-C

35416675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114367282-T-A

35416675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114367282-T-C

35416739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114367345-A-G

35416785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114367392-T-C

35416785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114367392-T-G

35416840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114367446-A-G

35416912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114367514-C-T

35416998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114367594-G-T

http://identifiers.org/hco/15/GRCh38#35417210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114367775-C-A

http://identifiers.org/hco/15/GRCh38#35417528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114368137-A-C

35418381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114368975-C-G

35418381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114368975-C-T

35418409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369003-T-C

35418813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369417-C-T

35418989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369598-C-G

35419024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369633-G-C

35419024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369633-G-T

35419069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369718-A-T

35419080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114369729-C-T

35419330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370050-A-G

35419375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370090-T-C

35421637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370474-A-G

35421656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370492-G-A

35421749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370576-T-G

35421791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370603-A-G

35422101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114370943-A-G

35422196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114371024-T-C

35422323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114371181-G-A

35422324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114371182-G-A

http://identifiers.org/hco/15/GRCh38#35425956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114372406-C-A

35426107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114372553-A-G

35426528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114372943-G-C

35426590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114373000-T-C

35426633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114373043-G-A

35426860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114373261-A-G

http://identifiers.org/hco/15/GRCh38#35427012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114373399-A-C

35427173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114373515-A-T

35427327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114373666-C-T

35427968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374334-C-G

35427968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374334-C-T

35428036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374394-G-T

35428707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374933-T-C

35428765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374987-T-A

35428765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114374987-T-C

35428845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375053-A-G

35428943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375150-T-C

35429045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375257-G-C

35429168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375361-G-A

35429256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375447-T-C

35429657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114375792-T-C

http://identifiers.org/hco/15/GRCh38#35430210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114376324-C-A

35430307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114376400-C-T

35430415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376512-A-T

35430534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376632-T-A

35430534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376632-T-C

35430581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376678-C-T

35430639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376736-T-C

35430743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114376834-G-A

35447452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114388986-C-T

35447608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114389139-A-G

35448094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114390443-T-C

35448388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114390729-T-C

35448497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114390842-C-T

35448604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114390951-T-C

35449522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114396763-G-A

35449686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114397498-A-G

35449820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114397606-A-G

35449928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114397692-T-A

35449928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114397692-T-C

35450005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114397770-C-T

http://identifiers.org/hco/15/GRCh38#35450025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114397786-C-A

35450315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114398013-G-A

35450544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114398281-G-C

35450544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114398281-G-T

35450561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114398301-T-A

35450660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114398376-C-T

35450782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114398498-C-G

35454865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114400067-A-T

35462945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114402325-T-C

35463278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114402616-G-A

35463932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403273-C-T

35463985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114403326-G-C

35465247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404261-G-A

35465750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404721-A-G

35465977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114404940-A-G

35475525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409118-G-A

35475774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114409366-A-G

35476924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410177-C-G

35476924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410177-C-T

35476999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410253-T-C

35477062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410316-A-T

35477544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410795-G-C

35477627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114410878-C-T

35477909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411161-G-A

35478527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411736-T-G

35478587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114411799-T-C

35478861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412059-G-A

35478926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412124-C-T

35479165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412361-T-G

http://identifiers.org/hco/15/GRCh38#35479179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114412375-C-A

35479276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412458-G-A

35479342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114412509-T-C

35479552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413153-T-C

35479708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413300-T-C

35479709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413301-G-A

35479730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413314-C-T

35479854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114413461-G-A

35480279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114414313-T-C

35485451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419196-C-T

35485553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419286-C-T

35485883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419542-C-T

35488721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419666-T-A

35488743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114419688-T-A

35489302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420276-G-A

35489306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420280-A-G

35489309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420283-G-C

35489319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420293-T-A

35489456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420445-A-G

35489509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420510-C-T

35489526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420527-A-G

35489526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420527-A-T

35489548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420566-T-C

http://identifiers.org/hco/15/GRCh38#35489592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114420611-C-A

35489592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420611-C-T

35489899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420904-T-C

35489899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114420904-T-G

35490185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114421195-T-C

35490278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421263-G-T

35490303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421288-A-G

35490304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421289-G-A

35490527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114421519-C-T

35492962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423736-T-C

35493033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423808-C-T

35493055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114423830-C-T

35493489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428002-T-A

35493511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428021-G-A

35493517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114428028-G-C

35497009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429646-T-G

35497198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429834-G-C

35497231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114429860-G-A

35497394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114430048-C-G

35497394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114430048-C-T

35497502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114430151-A-G

35497506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114430155-G-A

35498322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114431262-G-A

35498388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114431323-A-G

35498400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114431335-G-A

35498514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114431441-C-T

http://identifiers.org/hco/15/GRCh38#35498923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114431978-C-A

35499249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114432358-T-C

35500139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114432565-T-C

http://identifiers.org/hco/15/GRCh38#35500530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114432949-C-A

35501247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433339-T-C

35501715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433758-T-G

35501887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114433916-A-G

35502108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114434125-G-C

http://identifiers.org/hco/15/GRCh38#35502155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114434172-A-C

35502364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436678-T-A

35502364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436678-T-C

35502457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114436761-T-C

http://identifiers.org/hco/15/GRCh38#35502771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114436974-C-A

35502854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114437052-C-T

35503298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114437660-G-T

35503318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114437677-C-T

35503908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438215-A-G

35504105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438317-C-G

35504116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438328-C-T

35504281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438482-T-C

35504476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438666-T-C

35504516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438702-C-T

35504677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114438845-A-G

35504941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439097-G-A

http://identifiers.org/hco/15/GRCh38#35504958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114439114-C-A

35504968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439124-A-T

35504975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114439131-T-C

35506266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114440488-A-G

35507191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114441367-T-C

35507963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442052-G-A

http://identifiers.org/hco/15/GRCh38#35508092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114442221-C-A

35508350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114442471-C-G

http://identifiers.org/hco/15/GRCh38#35508417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114442528-A-C

35508971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443082-C-T

35509032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443141-T-C

35509032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443141-T-G

35509098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443207-C-T

35509363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114443461-A-G

35510322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444080-C-T

35510520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444284-C-T

35511004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444758-C-T

35511244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114444974-G-T

35511297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445025-T-C

35511307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445035-G-A

http://identifiers.org/hco/15/GRCh38#35511337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114445065-C-A

35511337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445065-C-T

35511338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445066-G-A

35511544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445336-G-A

35512131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114445934-T-C

http://identifiers.org/hco/15/GRCh38#35512238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114446036-C-A

35512346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446135-C-T

35512758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446521-T-C

35512762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446525-G-T

35512831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446590-T-A

35512879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446636-A-T

35513041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446794-C-G

35513077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114446825-A-G

35513647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114447447-C-T

35513658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114447459-G-A

35513686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114447481-A-G

35514338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448142-T-G

35514490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448304-G-C

35514490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448304-G-T

35514596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448387-A-G

35515147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114448855-G-A

35515262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449028-G-A

35516007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449381-T-C

35516042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449414-C-T

35516298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449637-G-A

35516301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449640-A-G

35516309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449648-T-C

35516361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449696-G-A

35516372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449707-T-C

35516651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114449997-T-C

35516860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114450171-G-T

35516948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114450254-G-A

35516991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114450295-A-G

35517026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114450319-C-T

35517029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114450322-C-T

35517846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451159-G-A

35518037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451326-T-A

35518052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451342-T-C

35518068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451363-A-G

35518156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451450-T-C

35518156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451450-T-G

35518344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114451624-G-A

35518848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114452013-G-A

35518848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114452013-G-T

http://identifiers.org/hco/15/GRCh38#35519646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114452886-A-C

35519672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114452912-C-T

35519884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114453113-G-C

http://identifiers.org/hco/15/GRCh38#35519941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#114453165-C-A

http://identifiers.org/hco/15/GRCh38#35520000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114453224-C-A

35520166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114453389-T-G

35520307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114453505-C-T

35520781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114453932-T-C

http://identifiers.org/hco/15/GRCh38#35520797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114453947-C-A

35520797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114453947-C-T

35520906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454063-T-C

35520972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454129-T-C

35520978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454135-A-G

35521039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454194-G-A

35521143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454297-T-C

35521224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454384-C-T

35521325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454470-T-A

35521325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454470-T-C

35521578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454709-T-C

35521583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454714-G-A

35521583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454714-G-T

http://identifiers.org/hco/15/GRCh38#35521807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114454937-C-A

35521807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454937-C-T

35521831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114454961-A-G

http://identifiers.org/hco/15/GRCh38#35521893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114455022-C-A

35521893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114455022-C-T

35521918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114455047-G-T

35521984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114455113-G-A

35521992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114455121-C-T

35522025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114455154-G-A

35522218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114455346-T-A

35522218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114455346-T-C

35522218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114455346-T-G

35522238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114455366-A-G

35522400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114455528-T-A

35522400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114455528-T-C

35522554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114455661-C-T

35522748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114455837-A-G

35522828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114455921-T-C

35523204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456241-T-C

35523208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456245-G-T

35523209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456246-C-T

35523561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456466-A-G

35523594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456498-G-T

35523766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114456662-T-C

35524112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457117-T-C

35524427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457476-T-C

35524439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457488-T-C

35524583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457581-C-T

35524640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457642-T-A

35524738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457699-A-G

35524848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114457769-G-A

35525175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114458055-G-A

http://identifiers.org/hco/15/GRCh38#35525194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114458073-A-C

35525633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114458536-A-G

35525949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114458863-G-C

35526018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114458929-G-A

35526049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114458960-T-C

35526125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114459037-G-A

35526142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114459046-T-C

35526182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114459103-C-T

35526647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114460132-G-C

35527935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114461379-T-C

35528031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114461474-C-T

35528097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114461536-T-A

35528297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114461793-T-G

35528449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114461939-T-A

http://identifiers.org/hco/15/GRCh38#35528487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114461973-C-A

35528595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114462082-T-A

35528600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114462087-T-C

35528606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114462093-C-T

35530686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466233-T-C

35530824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466369-C-T

35530835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466380-C-G

35530854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466399-C-G

35530854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466399-C-T

35531108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466652-C-T

35531321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466851-T-G

35531334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466870-T-A

35531336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466872-C-T

35531362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466897-T-C

35531456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114466996-T-G

35531463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467003-G-A

35531957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467202-G-A

35532116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467362-A-G

35532136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467380-T-G

35532193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467443-A-G

35532368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467574-G-A

35532433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114467619-T-C

35533124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114468026-T-A

35533205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114468114-C-T

35533214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114468123-G-A

35533474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114468396-C-G

http://identifiers.org/hco/15/GRCh38#35534633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114471712-C-A

35534633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114471712-C-T

35534891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114471982-C-T

35535091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114472150-G-A

35535116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114472173-T-G

35535127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114472184-T-A