170767933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33548014-G-A

170767939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33548008-G-A

170767961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547985-T-A

170767979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547963-C-T

170768039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547892-G-A

170768042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547889-A-G

170768120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547818-G-A

170768157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547781-A-T

170768200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547735-G-T

170768215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547720-C-T

170768234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547701-G-A

170768258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547678-T-C

170768268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547668-C-T

170768322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547614-C-T

170768450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547509-C-G

http://identifiers.org/hco/5/GRCh38#170768538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33547471-A-C

170768584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547428-G-A

170768649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547368-A-T

170768833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547219-A-G

170769027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33547032-T-G

170769332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546741-G-A

170769394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546672-A-G

170769448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546619-A-G

170769459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546608-T-A

http://identifiers.org/hco/5/GRCh38#170769488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33546580-A-C

170769488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546580-A-G

170769592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33546483-T-G

170769696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33546383-A-G

170769731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33546351-G-A

http://identifiers.org/hco/5/GRCh38#170769732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33546350-C-A

170769737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33546345-G-A

170769737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33546345-G-C

http://identifiers.org/hco/5/GRCh38#170771328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33544935-C-A

170771408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544837-A-G

170771516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544758-G-T

170771527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544747-A-T

170771593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544690-G-T

170771612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544671-T-C

170771794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544532-C-G

170771798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544528-A-G

170771803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544523-G-C

http://identifiers.org/hco/5/GRCh38#170771876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33544482-A-C

170771876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544482-A-G

170771960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544431-C-T

170772046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33544355-G-A

170772655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 33543559-G-T

http://identifiers.org/hco/5/GRCh38#170772660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33543554-C-A

170772660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543554-C-T

170772664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543550-T-C

170772669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543544-T-C

http://identifiers.org/hco/5/GRCh38#170772670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33543543-C-A

170772670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543543-C-T

170772678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543535-G-A

170772678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543535-G-T

170772685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543528-T-A

170772685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543528-T-C

170772754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543459-G-T

170772943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543284-T-C

170772967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543260-A-G

170773052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543212-C-T

170773183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543116-T-G

170773190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543109-G-T

170773300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33543008-T-A

http://identifiers.org/hco/5/GRCh38#170773586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33542669-A-C

170773807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33542452-C-G

170773807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33542452-C-T

170774040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33541289-G-A

170774051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33541278-C-T

170774154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33541193-G-T

170778471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33533341-C-T

170778501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33533323-G-A

170778630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33533197-G-A

170778647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33533186-T-C

http://identifiers.org/hco/5/GRCh38#170781373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33532220-A-C

170781384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532209-A-G

170781384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532209-A-T

170781432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532159-A-G

170781469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532113-T-C

170781489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532087-T-C

170781515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33532061-A-T

170781574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33531998-G-C

http://identifiers.org/hco/5/GRCh38#170781725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33531853-C-A

170782389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33530098-T-C

http://identifiers.org/hco/5/GRCh38#170782577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33529914-C-A

170782577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33529914-C-T

170782622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33529863-G-A

170782624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33529861-A-G

170782739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33529726-G-A

170782739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33529726-G-T

170783808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33528859-G-A

170783808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33528859-G-T

170783822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33528845-T-C

170783911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528768-G-A

170783935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528745-A-G

170784205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528489-A-T

170784634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528260-A-T

170784694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528198-A-G

170784713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33528171-G-T

170785141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33527841-T-C

170785586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33527192-G-A

170785742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33527032-G-A

http://identifiers.org/hco/5/GRCh38#170785763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33527011-C-A

170785763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33527011-C-T

170786151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33526382-A-T

170786160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33526373-G-T

170786238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33526298-A-G

http://identifiers.org/hco/5/GRCh38#170786677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33525824-A-C

170786677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33525824-A-T

170786801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33525691-T-C

170787548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33524224-G-A

http://identifiers.org/hco/5/GRCh38#170787721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33524063-C-A

http://identifiers.org/hco/5/GRCh38#170788178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523779-C-A

http://identifiers.org/hco/5/GRCh38#170788183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523774-C-A

170788183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523774-C-T

170788189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523768-A-T

170788228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523724-A-G

170788246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523719-G-T

170788257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523710-G-A

170788257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523710-G-T

170788287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523681-T-C

170788288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523680-G-A

170788288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33523680-G-T

http://identifiers.org/hco/5/GRCh38#170788409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523576-A-C

170788409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523576-A-G

170788409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523576-A-T

170788449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523538-A-G

170788453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523534-A-G

http://identifiers.org/hco/5/GRCh38#170788468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523519-C-A

170788468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523519-C-T

http://identifiers.org/hco/5/GRCh38#170788500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523489-C-A

http://identifiers.org/hco/5/GRCh38#170788507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523482-A-C

170788507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523482-A-G

170788507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523482-A-T

http://identifiers.org/hco/5/GRCh38#170788518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523471-A-C

170788518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523471-A-G

170788518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33523471-A-T

170788555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 33523437-C-G

170788673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33523311-G-A

170788745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33523239-C-T

http://identifiers.org/hco/5/GRCh38#170788788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523195-C-A

170788788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33523195-C-G

170788788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33523195-C-T

http://identifiers.org/hco/5/GRCh38#170788803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33523180-C-A

170788803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33523180-C-T

170788931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33522690-T-C

170788950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33522670-A-T

http://identifiers.org/hco/5/GRCh38#170789027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33522584-C-A

170789027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33522584-C-T

170789130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 33522488-A-T

170789385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522244-G-A

170789387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522242-T-C

170789388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522241-G-T

170789397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522232-T-C

170789464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522164-C-T

170789503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522124-A-G

170789564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522070-A-G

170789570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522064-C-T

170789575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522059-T-A

170789575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33522059-T-C

170789675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521957-C-T

170789678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521954-A-G

170789731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521913-T-A

170789731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521913-T-C

http://identifiers.org/hco/5/GRCh38#170789921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33521743-C-A

170789930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521734-C-T

170789954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521709-T-C

170789996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521679-C-T

170790009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521666-C-G

170790726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521363-T-A

170790729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521360-A-G

http://identifiers.org/hco/5/GRCh38#170790787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33521303-C-A

170790796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521293-G-A

170790834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521246-G-A

170790973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521121-A-G

170791081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33521029-C-T

170791113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520999-C-T

170791139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520971-G-T

170791231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520879-C-T

170791277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520853-A-G

http://identifiers.org/hco/5/GRCh38#170791360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33520779-C-A

170791360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520779-C-T

http://identifiers.org/hco/5/GRCh38#170791412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33520725-C-A

170791529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520619-T-C

170791752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520387-C-T

170791857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520297-T-C

170792008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33520166-G-A

170792918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33519694-T-A

170792919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33519693-G-C

http://identifiers.org/hco/5/GRCh38#170793562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33519172-C-A

170793562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33519172-C-T

170793703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33519031-T-C

170793917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33518535-A-G

170794088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33518339-C-T

170794177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33518209-A-G

170794177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33518209-A-T

170794309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33518054-T-C

170794348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33518017-T-A

170794348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33518017-T-C

170794426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517980-A-G

170794911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517633-A-G

170794962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517588-T-C

170795109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517521-G-T

http://identifiers.org/hco/5/GRCh38#170795144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33517486-C-A

170795144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517486-C-T

http://identifiers.org/hco/5/GRCh38#170795197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33517437-C-A

170795197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517437-C-G

170795197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517437-C-T

170795334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: 33517302-G-A

170795334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: 33517302-G-C

http://identifiers.org/hco/5/GRCh38#170795385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33517251-A-C

170795551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33517086-T-C

http://identifiers.org/hco/5/GRCh38#170795575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33517060-C-A

170795694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33516935-C-G

170795695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33516934-C-T

170795719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33516903-A-T

170795819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33516063-G-A

170795858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33516028-T-G

http://identifiers.org/hco/5/GRCh38#170796136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33515728-A-C

170796269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515597-C-G

170796421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515464-T-C

170796552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515378-T-A

170796721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515228-G-C

170796731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515218-A-G

170796749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33515203-T-A

170796987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33514994-A-G

170797436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33514021-A-T

170797479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: 33513933-G-A

170797560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513852-T-A

170797560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513852-T-C

170797599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513812-G-A

170797599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513812-G-T

http://identifiers.org/hco/5/GRCh38#170797625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33513789-A-C

170797663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513762-G-A

170797663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513762-G-T

170797700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513725-T-C

170797956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513478-A-G

170797980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513454-T-C

170798490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513276-C-T

170798492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33513274-A-G

170801709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33511305-A-G

170801774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33511240-T-G

170802063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33510835-T-C

170802073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33510825-A-T

170802638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33510282-A-G

170803088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33509644-G-A

170803234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33509557-G-A

170803444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33509349-G-T

170804620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33508022-T-C

170804666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507986-T-C

170804745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507911-C-T

170804783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507860-A-G

170804899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507754-C-T

170805393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507363-T-A

170805583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507193-G-A

170805583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507193-G-T

170805694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507087-A-G

http://identifiers.org/hco/5/GRCh38#170805700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33507081-C-A

170805700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33507081-C-T

170805709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 33507072-T-C

http://identifiers.org/hco/5/GRCh38#170805805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33506976-A-C

170805805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense variant
orthologous variants: 33506976-A-G

http://identifiers.org/hco/5/GRCh38#170805930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33506802-C-A

170805930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506802-C-T

170805931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506801-G-A

170805931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506801-G-T

http://identifiers.org/hco/5/GRCh38#170805955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33506693-A-C

170805955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506693-A-G

170806308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506377-G-A

170806308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33506377-G-C

170808290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505436-A-G

170808382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505351-C-T

170808398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505320-G-C

170808431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505289-C-T

170808437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505283-A-G

http://identifiers.org/hco/5/GRCh38#170808455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33505265-C-A

http://identifiers.org/hco/5/GRCh38#170808549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33505170-C-A

http://identifiers.org/hco/5/GRCh38#170808551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33505168-C-A

http://identifiers.org/hco/5/GRCh38#170808558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33505160-C-A

170808562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505156-A-G

170808577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505141-C-G

170808577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505141-C-T

170808589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33505129-T-C

170808847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504959-A-G

170808847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504959-A-T

170809328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504737-A-T

http://identifiers.org/hco/5/GRCh38#170809470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33504594-C-A

170809470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504594-C-T

170809497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504571-G-A

170809857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33504212-G-T

170810550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33503770-C-T

170811364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33503212-A-G

170811553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: intron variant
orthologous variants: 33503037-A-T

170811961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 33502835-A-G

http://identifiers.org/hco/5/GRCh38#170812025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33502771-C-A

170812025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 33502771-C-G

170812025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 33502771-C-T

170812096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 33502700-C-T

170812359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502458-A-G

170812359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502458-A-T

170812436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502416-T-C

170812522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502310-A-T

http://identifiers.org/hco/5/GRCh38#170812667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33502176-A-C

170812700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502143-G-T

170812743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502098-G-A

170812743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33502098-G-C

http://identifiers.org/hco/5/GRCh38#170812764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33502077-A-C

170812958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501912-G-C

170813096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501780-T-C

170813120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501756-A-G

170813128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501748-A-G

http://identifiers.org/hco/5/GRCh38#170813236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33501640-C-A

170813477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501402-A-G

170813478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501401-G-A

170813478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501401-G-T

170813486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501393-G-A

170813486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501393-G-T

170813491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501388-A-G

170813504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501375-T-C

http://identifiers.org/hco/5/GRCh38#170813525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#33501367-C-A

170813525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501367-C-T

170813528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33501364-C-T

170813875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33500936-G-T

170813899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33500912-G-T

170813919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33500892-T-C

170814035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4089
most severe consequence: 3 prime UTR variant
orthologous variants: 33500774-G-C