http://identifiers.org/hco/3/GRCh38#100492760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56706335-C-A

http://identifiers.org/hco/3/GRCh38#100492766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56706329-C-A

100492766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5 prime UTR variant
orthologous variants: 56706329-C-T

100493060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56706038-C-T

100493149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56705967-C-G

100493149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56705967-C-T

100495042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56704932-C-T

http://identifiers.org/hco/3/GRCh38#100495119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56704866-A-C

100495348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56704478-T-A

100495385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56704442-C-G

100495908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56703946-A-G

100496142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56703771-G-A

100496320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56703592-G-A

100496375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56703532-G-A

http://identifiers.org/hco/3/GRCh38#100496407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56703500-A-C

100496789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702971-G-A

100500142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702419-A-G

100500345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702233-G-A

100500418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702215-A-G

http://identifiers.org/hco/3/GRCh38#100500565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56702103-A-C

100500565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702103-A-G

http://identifiers.org/hco/3/GRCh38#100500633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56702034-C-A

100500633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702034-C-T

100500644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56702022-A-G

100500767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56701903-G-T

100500901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56701767-C-T

http://identifiers.org/hco/3/GRCh38#100501005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56701714-A-C

100501597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56701377-A-G

100501603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56701372-C-G

http://identifiers.org/hco/3/GRCh38#100501705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56701297-A-C

100501785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56700613-C-T

100501890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56700509-A-G

100502863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698956-A-G

100503580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698605-G-C

100503624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698566-A-G

100503626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698564-G-C

100504029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698224-A-G

100504078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698175-T-C

100504150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698112-A-G

100504242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56698029-A-G

100505017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56693418-T-C

100505229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56693177-C-G

100505704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692687-G-A

100505819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692594-G-A

100505995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692427-G-A

100506094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692076-G-A

100506094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692076-G-C

100506094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56692076-G-T

100506442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56691667-C-G

100506442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56691667-C-T

100506992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56691189-G-T

100507294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56690928-C-T

100507624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56690701-A-G

http://identifiers.org/hco/3/GRCh38#100507767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56690570-A-C

100516439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56690189-G-T

100518632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688606-C-T

100518751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688483-T-C

http://identifiers.org/hco/3/GRCh38#100518776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56688459-C-A

100518776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688459-C-G

100518776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688459-C-T

100518933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688291-T-C

100519056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688177-G-A

100519056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56688177-G-T

100519080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56688153-G-T

100519157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56688075-A-G

100519158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56688074-G-A

100519158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56688074-G-T

100519165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56688067-G-A

100519321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687919-G-T

http://identifiers.org/hco/3/GRCh38#100519350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56687890-C-A

100519397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687834-G-A

100522622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56676000-A-T

100522915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56675713-T-C

100523320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56675343-T-C

100523445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56675201-G-C

100523854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674978-C-T

100523879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674953-G-A

100523963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674850-G-A

http://identifiers.org/hco/3/GRCh38#100524276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56674588-A-C

100524598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674355-A-T

100525808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56673751-G-C

100526050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56673549-T-C

100526335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56673266-C-T

100527406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671776-T-C

100527436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671752-G-C

100527567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671627-T-C

100527701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671497-C-T

http://identifiers.org/hco/3/GRCh38#100527720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56671478-C-A

100527720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671478-C-T

100528155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670981-G-A

100528383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670780-G-A

100528540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670621-T-G

100528608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670566-C-T

100528676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670497-C-T

100529019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670207-T-C

100529167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56670148-A-G

100529392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669949-T-G

100529488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669852-T-G

100530914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56666447-T-G

100531573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665833-A-G

100531588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665807-A-G

100532242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664495-G-A

100532314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664425-G-T

100533370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663648-A-T

100533388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663634-C-T

100533548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663487-C-T

100533566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663469-G-T

100533749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663320-G-A

100533884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663193-C-T

100534032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662957-A-G

100534207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662781-G-A

http://identifiers.org/hco/3/GRCh38#100534295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56662692-A-C

100534443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662546-C-T

100534543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662477-A-G

100534695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662333-C-G

100534842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662216-G-A

100535239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661925-G-C

100535240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661924-C-G

100535388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661898-A-G

100535544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661745-A-G

http://identifiers.org/hco/3/GRCh38#100535621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56661684-C-A

100535621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661684-C-T

100535688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661617-C-G

100535688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661617-C-T

100535867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661460-T-C

100536063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660184-T-C

100536149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660088-G-A

100536186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660066-A-T

100536338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659912-A-G

100536361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659889-T-C

100536439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659830-C-T

100536575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659715-T-C

100536592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659698-A-G

100537620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659457-G-C

100537855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659155-A-G

100537855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659155-A-T

100537891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659114-G-C

100548600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652812-A-G

http://identifiers.org/hco/3/GRCh38#100548619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56652793-A-C

100548772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652661-A-G

100549403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652386-C-T

100549475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652328-C-T

100549700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652156-A-G

100550225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652112-T-A

100550336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652001-A-G

100550619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651723-C-G

http://identifiers.org/hco/3/GRCh38#100551727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56650941-C-A

100551763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650914-G-A

100551794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650880-A-G

100551794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650880-A-T

http://identifiers.org/hco/3/GRCh38#100551840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56650842-A-C

100552092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650625-A-T

100552093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650624-T-G

100552253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650437-T-A

100552292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650394-A-T

100552321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650363-G-T

100552859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649832-G-A

100553286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648121-C-T

100553300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648107-T-A

100553305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648102-T-C

100553546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647788-A-G

100553572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647761-G-A

100553687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647654-C-T

100553952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647410-C-T

100554038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647335-C-T

100554203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647174-A-G

100554227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647150-T-C

100554497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646850-A-G

100554617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646730-T-G

100554618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646729-A-G

100554652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646695-T-C

100554821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646527-A-G

100554841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646514-T-C

100555013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646356-T-C

100555153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646259-G-A

100555153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646259-G-C

100555159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646253-A-G

100555201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56646227-A-G

100555348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56646080-T-A

100555495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56645399-T-C

100555652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56645240-A-T

100555897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644507-T-C

100556626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644083-G-A

100556626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644083-G-T

100556792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56643923-C-T

100557013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56643703-G-T

100557235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56643476-G-A

100558209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56642965-G-A

100558302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56642861-A-G

100558792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56642405-C-G

100559325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56641615-C-T

100559951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56640432-A-G

100560767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56639733-C-T

100561135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56639378-G-C

100561534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56639003-C-T

100562064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56638315-C-T

100562097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56638282-A-G

100562393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56637993-T-C

100568211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632760-G-A

100568263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632712-T-C

100568287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632688-A-G

100568487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632518-A-G

100568547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632357-A-G

100568661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632177-A-G

100568688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632151-G-A

100568689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632150-A-T

100568750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632101-G-A

100568764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron variant
orthologous variants: 56632087-A-G

100569070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631783-A-G

100569087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631766-G-A

100569087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631766-G-T

100569089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631764-T-A

100569089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631764-T-C

http://identifiers.org/hco/3/GRCh38#100569229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56631632-A-C

100569316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631559-T-C

100569470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631426-C-T

100569667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631256-A-G

100570083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630900-T-C

http://identifiers.org/hco/3/GRCh38#100570704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56630337-C-A

100570704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56630337-C-T

100570820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56630220-C-T

100574646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56630005-A-G

100574658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56629995-G-T

100574667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56629986-T-C

100575919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627497-T-C

100575985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627438-C-T

100575996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627427-C-T

100575997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627426-G-A

100576781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627289-A-G

100576785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627285-C-T

http://identifiers.org/hco/3/GRCh38#100576787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56627283-A-C

100576787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627283-A-G

100576861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56627202-G-T

100576962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56627100-G-A

100577055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56627016-T-C

http://identifiers.org/hco/3/GRCh38#100577090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56626976-C-A

100577090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626976-C-G

100577094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626972-T-G

100577103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626963-A-G

100577202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626868-T-G

100577284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626790-G-A

100577284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626790-G-T

100577361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626717-T-C

100577372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25480
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56626706-T-C