27545928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146953825-C-G

27546046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146953945-G-A

27546112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954003-G-A

27546540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954391-T-A

27546622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954470-C-T

http://identifiers.org/hco/13/GRCh38#27546745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146954558-C-A

27546748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954561-G-T

27546770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954583-C-G

27546788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146954601-T-C

27547188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955002-C-T

27547282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955090-A-G

http://identifiers.org/hco/13/GRCh38#27547415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146955213-A-C

http://identifiers.org/hco/13/GRCh38#27547427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146955225-A-C

27547450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955249-A-T

27547510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955307-A-G

http://identifiers.org/hco/13/GRCh38#27547531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146955328-C-A

27547531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955328-C-T

27547712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955407-T-C

27547712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955407-T-G

http://identifiers.org/hco/13/GRCh38#27547728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146955427-C-A

27547728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955427-C-T

27547758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955448-A-G

27547762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955453-G-A

27547762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955453-G-T

27547789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955469-G-A

27547911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955476-G-A

27547911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955476-G-C

27547911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955476-G-T

27548130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955586-T-C

27548130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955586-T-G

27548138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955593-T-A

27548138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955593-T-C

27548212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955632-T-C

27548212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955632-T-G

27548235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955648-G-A

27548235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955648-G-T

27548288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 3 prime UTR variant
orthologous variants: 146955687-A-G

27549884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956433-T-C

27550089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956619-A-T

27550200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956710-G-A

27550200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956710-G-T

http://identifiers.org/hco/13/GRCh38#27550234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146956740-A-C

27550234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956740-A-G

http://identifiers.org/hco/13/GRCh38#27550260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146956751-C-A

27550260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956751-C-T

27550310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956794-T-C

27550311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956795-C-G

27550317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146956801-T-C

27550344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146956828-A-T

27550347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146956831-A-G

27550396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146956880-T-C

27550467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146956951-T-G

27550479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146956963-G-A

27550491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 146956975-G-A

27551427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146958108-G-A

http://identifiers.org/hco/13/GRCh38#27551470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146958151-C-A

27552474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146960503-C-T

27552546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146960566-C-G

27552547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146960567-A-T

27552802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146960751-T-G

http://identifiers.org/hco/13/GRCh38#27552854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146960833-C-A

27552904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146960903-A-G

http://identifiers.org/hco/13/GRCh38#27553121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146961081-C-A

27553121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961081-C-T

27553156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961112-G-A

27553156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961112-G-T

27553345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146961299-A-G

27553447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 146961401-G-A

27553447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 146961401-G-T

27553472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961425-G-A

27553472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961425-G-T

27553491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961448-T-C

http://identifiers.org/hco/13/GRCh38#27553523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146961475-A-C

27553523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961475-A-G

27553570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961523-G-A

27553570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961523-G-C

27553577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146961530-T-C

http://identifiers.org/hco/13/GRCh38#27553822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146961761-C-A

27555540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146963292-T-G

27555692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146963439-T-C

27555760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146963501-T-C

27555865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146963608-G-A

27556154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146963937-T-C

27556351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146964132-T-C

27556351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146964132-T-G

27559363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964362-A-G

27559364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964363-T-C

27559398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964397-T-C

27559523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964524-T-G

27559741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964755-A-T

27559774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964791-A-T

http://identifiers.org/hco/13/GRCh38#27559797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146964813-C-A

27559797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146964813-C-T

27559872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146964893-T-C

http://identifiers.org/hco/13/GRCh38#27560009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146965021-C-A

27560009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965021-C-T

27560045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965050-T-C

27562357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965856-T-C

27562360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965859-T-C

27562360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965859-T-G

27562402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146965886-A-G

27562461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146965945-C-T

27562503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146965987-G-A

27562595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, missense_variant
orthologous variants: 146966079-C-G

27562638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146966122-T-C

27562638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146966122-T-G

27562650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146966134-A-G

27562653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146966137-A-G

27562758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 146966242-A-G

27562783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 146966276-T-A

27562783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 146966276-T-C

27562811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966312-G-A

27562811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966312-G-C

http://identifiers.org/hco/13/GRCh38#27562813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146966319-C-A

27562813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966319-C-T

http://identifiers.org/hco/13/GRCh38#27562868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146966374-C-A

27562997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966468-A-G

27563498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966883-C-T

27563595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146966976-G-T

27563704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967109-G-C

27563764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967184-C-G

27563940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967357-G-A

27563965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967378-C-T

http://identifiers.org/hco/13/GRCh38#27564207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146967575-C-A

27564207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967575-C-T

27564310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967674-T-C

27564435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967777-A-T

27564464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967803-T-C

27564549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967883-G-A

http://identifiers.org/hco/13/GRCh38#27564587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146967922-C-A

27564587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146967922-C-T

27564682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146968014-C-T

27564760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146968117-T-A

27564761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146968118-C-T

27564782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146968139-C-G

27567586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146969669-G-C

27567667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146969712-T-C

27567817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146969862-T-A

27567817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146969862-T-C

27568956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970013-A-G

27568969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970029-G-A

27568969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970029-G-T

http://identifiers.org/hco/13/GRCh38#27568993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970053-A-C

27568993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970053-A-G

27568997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970057-A-G

http://identifiers.org/hco/13/GRCh38#27569057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970117-A-C

27569057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146970117-A-G

27569098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970158-A-G

http://identifiers.org/hco/13/GRCh38#27569142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970196-A-C

27569142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970196-A-G

27569161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970215-A-G

27569163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970217-A-G

http://identifiers.org/hco/13/GRCh38#27569169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970223-C-A

27569169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970223-C-T

27569251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146970305-C-T

http://identifiers.org/hco/13/GRCh38#27569319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970376-C-A

27569331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970388-T-A

27569331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970388-T-C

27569339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970408-G-C

27569343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970412-G-A

27569343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970412-G-C

27569352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970428-T-A

27569352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970428-T-C

http://identifiers.org/hco/13/GRCh38#27569362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146970448-A-C

27569402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970481-A-G

27569403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970482-T-C

27569403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970482-T-G

27569409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970488-T-C

27569643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970697-C-G

27569643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970697-C-T

27569644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146970698-A-T

27570399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146971184-A-G

27570440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146971212-C-T

27570449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146971221-A-G

27570462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146971237-G-A

27571455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146973765-A-G

27571467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146973777-G-A

http://identifiers.org/hco/13/GRCh38#27571595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146973911-C-A

27571595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146973911-C-T

27571767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146974027-C-T

27571788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146974048-G-C

http://identifiers.org/hco/13/GRCh38#27572127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146974342-A-C

27572174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146974389-G-A

27572428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975377-G-A

27572428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975377-G-C

27572562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975482-G-A

27572624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975545-C-G

27572624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975545-C-T

27572721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975628-C-T

http://identifiers.org/hco/13/GRCh38#27572838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146975719-C-A

27573069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146975923-T-C

27580677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978090-T-C

27580719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978130-T-G

http://identifiers.org/hco/13/GRCh38#27580792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146978210-C-A

27580833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978354-C-T

27580865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978390-A-G

27580965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978469-T-C

27581036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978549-A-G

27581163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978667-G-A

27581163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978667-G-C

27581163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978667-G-T

27581291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146978835-G-T

27581350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146978894-T-C

http://identifiers.org/hco/13/GRCh38#27581376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146978920-A-C

27581405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: missense variant
orthologous variants: 146978949-C-G

http://identifiers.org/hco/13/GRCh38#27581449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146978993-C-A

27581449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146978993-C-G

27581449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146978993-C-T

27581590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146979134-G-A

27581595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: synonymous variant
orthologous variants: 146979139-A-G

http://identifiers.org/hco/13/GRCh38#27581741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146979288-A-C

27582413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146979490-G-A

27582436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146979513-C-T

27582922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146979788-G-A

27583117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146979967-T-C

27583140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146979986-T-A

27583635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980089-C-T

27583668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980120-T-C

http://identifiers.org/hco/13/GRCh38#27583792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146980234-C-A

27583792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980234-C-T

27583819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980260-T-C

27584011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980484-T-C

27584078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980559-C-G

http://identifiers.org/hco/13/GRCh38#27584133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146980605-C-A

http://identifiers.org/hco/13/GRCh38#27584206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146980653-C-A

27584206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980653-C-T

27584339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980743-T-C

27584339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980743-T-G

27584496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980854-G-C

27584503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980861-T-C

http://identifiers.org/hco/13/GRCh38#27584665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146980958-A-C

27584665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980958-A-G

27584675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980968-G-A

27584675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146980968-G-C

27584765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146981056-A-G

27585568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146981175-A-G

27585833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146981396-G-A

27589300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146984018-T-G

27589309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146984027-T-C

27590833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146985880-T-C

27590850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146985897-A-G

http://identifiers.org/hco/13/GRCh38#27590880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146985924-A-C

27590882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146985926-G-A

27591122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986058-G-T

27591194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986120-C-T

27591313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986227-A-T

27591525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986406-C-T

27591536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986417-T-C

27591617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986481-T-A

27591617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146986481-T-C

27599053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990060-T-C

27599081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990115-T-C

27599157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990178-G-A

27599159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990180-C-G

27599475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990451-C-T

27599591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146990529-T-C

27599752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146991543-C-T

27599786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146991583-T-C

27599973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146991767-A-G

27600010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146991800-A-G

27600025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146991815-T-A

27600025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146991815-T-C

27600069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146991856-A-G

http://identifiers.org/hco/13/GRCh38#27600115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#146991902-C-A

27600585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146992788-G-A

27601189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146993524-A-G

27601249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146993565-C-G

27601406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146993711-A-G

27601517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146993794-G-A

27602694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146994620-A-G

27602867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146994772-A-G

27603239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146995409-C-G

27603266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146995437-T-C

27603442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146995599-A-G

27603547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146995702-C-G

27603797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146995921-C-T

27604496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146996458-A-G

27604501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146996462-T-A

27605416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146997769-C-T

27605612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146997944-C-T

27605668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146997984-T-C

27605762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146998069-T-C

27605791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146998098-A-G

27605795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 146998102-T-C

http://identifiers.org/hco/13/GRCh38#27605880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146998363-C-A

27606025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146998486-T-C

27606172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146998632-G-A

27606172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146998632-G-T

27606228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146998695-G-C

http://identifiers.org/hco/13/GRCh38#27606419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#146999179-C-A

27606903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146999827-A-G

27606929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146999861-T-A

27606929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 146999861-T-C

27607091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000034-T-C

27607204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000145-A-G

http://identifiers.org/hco/13/GRCh38#27607526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147000431-A-C

27607526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000431-A-G

27607693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000576-T-C

27607814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000745-T-A

27607819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000750-T-C

27607826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000760-G-A

27607918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147000842-A-G

27609903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004559-C-T

27609904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004560-G-A

27609999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004830-C-G

27610059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004891-T-C

27610168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004974-C-T

27610188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147004993-A-G

27610234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005037-G-A

27610279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005248-T-C

27610303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005274-C-T

27610305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005276-G-C

27610315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005286-C-T

27610336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005313-A-G

27610410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005393-C-T

27610496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005463-T-C

27610581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005555-C-T

http://identifiers.org/hco/13/GRCh38#27610688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147005632-C-A

27610691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005635-C-T

27610934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005874-C-G

27610957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005901-T-C

27610971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005906-T-C

27611006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147005937-G-C

http://identifiers.org/hco/13/GRCh38#27611226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147006133-A-C

27611341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006247-C-G

27611377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006280-C-T

27611385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006288-T-C

27611450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006353-G-A

27611450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006353-G-C

27611470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006370-T-C

27611692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006551-C-G

27611745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006601-T-C

27611854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006722-T-A

27611854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006722-T-C

27611974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006825-G-T

27612088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006939-A-G

27612106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147006957-C-T

27612209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007042-T-C

27612270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007103-C-T

http://identifiers.org/hco/13/GRCh38#27612469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147007259-A-C

27612494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007288-A-G

27612921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007565-T-C

27612930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007574-C-T

27613269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147007857-G-A

27613406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147008005-G-C

27617604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147010541-G-A

27617848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147010757-T-C

27617878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147010786-C-T

27617971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147010881-T-C

http://identifiers.org/hco/13/GRCh38#27617998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147010917-C-A

27618036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147010954-C-G

27618172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011261-C-G

27618172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011261-C-T

27618402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011458-C-G

27618490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011508-C-G

27618769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011775-C-T

27618797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147011803-C-T

27619051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012023-G-A

http://identifiers.org/hco/13/GRCh38#27619106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147012080-A-C

27619262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012221-T-C

27619292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012253-G-A

27619292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012253-G-T

27619370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012337-T-C

27619582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012618-T-C

27619877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147012908-G-T

http://identifiers.org/hco/13/GRCh38#27620254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013158-C-A

27620254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147013158-C-T

http://identifiers.org/hco/13/GRCh38#27620450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013256-C-A

27620450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013256-C-T

27620455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013261-T-C

http://identifiers.org/hco/13/GRCh38#27620476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013277-C-A

27620476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147013277-C-T

http://identifiers.org/hco/13/GRCh38#27620490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013291-C-A

27620490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147013291-C-G

27620490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 147013291-C-T

27620540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 147013326-A-G

27620540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 147013326-A-T

27620619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147013407-G-A

27620619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147013407-G-C

27620619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: 147013407-G-T

http://identifiers.org/hco/13/GRCh38#27620623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013411-C-A

27620623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 147013411-C-T

27620665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron_variant, undefined
orthologous variants: 147013454-C-T

http://identifiers.org/hco/13/GRCh38#27620679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013467-A-C

27620824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013593-G-A

27620824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013593-G-T

http://identifiers.org/hco/13/GRCh38#27620837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#147013606-C-A

27620837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013606-C-T

27620876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013648-G-A

27620894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013656-A-G

27620894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20421
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 147013656-A-T