http://identifiers.org/hco/3/GRCh38#13549176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91189842-C-A

13549176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 5 prime UTR variant
orthologous variants: 91189842-C-T

http://identifiers.org/hco/3/GRCh38#13549191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91189857-C-A

13549191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 5 prime UTR variant
orthologous variants: 91189857-C-G

13549191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 5 prime UTR variant
orthologous variants: 91189857-C-T

13549634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91190031-C-T

13549843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91190183-T-G

http://identifiers.org/hco/3/GRCh38#13550167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91190449-A-C

http://identifiers.org/hco/3/GRCh38#13550335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91190597-C-A

13550741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191006-C-G

13551071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191331-G-A

13551204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191441-C-T

13551283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191505-G-A

13551283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191505-G-T

13551292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191513-C-G

13551363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191582-G-A

13551455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191673-G-T

http://identifiers.org/hco/3/GRCh38#13551649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91191854-C-A

13551658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91191863-A-G

13553022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195111-G-C

13553246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195317-G-A

13553359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195355-G-A

13553434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195421-G-A

13553447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195434-G-A

13553519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195468-C-G

13553519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195468-C-T

13553555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195504-G-A

13553555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195504-G-C

13553597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91195548-A-G

13557947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91197028-G-A

13557978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91197072-G-A

13557978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91197072-G-C

13558619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91198720-T-C

http://identifiers.org/hco/3/GRCh38#13558635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91198736-A-C

13558635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91198736-A-G

13558635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91198736-A-T

13558713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91198812-C-T

13559058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91199186-G-T

13559271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91199323-G-A

13559294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91199346-C-T

13560474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200464-T-C

13560544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200582-T-G

13560573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200608-C-T

13560667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200700-C-T

13561079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200944-T-C

13561094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91200959-C-T

13561341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201229-T-C

13561363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201239-A-T

13561425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201259-C-G

13561583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201399-C-G

13561627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201449-T-C

http://identifiers.org/hco/3/GRCh38#13561711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91201550-C-A

13561711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91201550-C-G

13561987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202025-A-G

13562002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202040-G-A

13562198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202209-G-T

13562374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202334-T-G

13562442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202355-C-T

13562549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202459-G-A

13562556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91202466-C-T

http://identifiers.org/hco/3/GRCh38#13563588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91203421-C-A

13563734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91203545-G-A

13563865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91203634-T-G

13564320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91203990-T-C

13564536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91204189-A-G

13564688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91204986-C-T

13564785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91205078-C-T

13565007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91205245-C-G

13565027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91205265-C-T

13569181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209107-G-A

13569181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209107-G-T

13569871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209650-C-T

13569966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209741-G-A

13570168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209894-T-C

13570185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209912-T-C

13570185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209912-T-G

13570187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209919-T-C

13570204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209937-G-A

13570204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209937-G-T

http://identifiers.org/hco/3/GRCh38#13570221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91209953-C-A

13570221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91209953-C-T

http://identifiers.org/hco/3/GRCh38#13570310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91210040-C-A

13570310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91210040-C-T

http://identifiers.org/hco/3/GRCh38#13570362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91210061-C-A

13570362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91210061-C-G

13570362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210061-C-T

http://identifiers.org/hco/3/GRCh38#13570574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#91210273-C-A

13570574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210273-C-T

13570643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210342-T-C

13570751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210450-A-T

http://identifiers.org/hco/3/GRCh38#13570757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#91210456-C-A

13570757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210456-C-T

13570847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210546-C-T

13570967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210666-C-T

13571072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210756-G-A

13571090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210774-C-T

13571180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210864-G-A

13571180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91210864-G-T

13571201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91210885-G-A

13571201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91210885-G-T

13571509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91211169-C-T

http://identifiers.org/hco/3/GRCh38#13571550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91211210-A-C

13571550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91211210-A-G

13571572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91211244-C-T

13571573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91211245-C-T

13571687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211361-G-T

13571694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211369-T-C

13571702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211377-G-T

http://identifiers.org/hco/3/GRCh38#13571712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91211387-C-A

13571712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211387-C-G

13571712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211387-C-T

13571722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211411-G-T

13571736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211421-G-A

13571736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211421-G-T

13571765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211448-T-C

13571765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211448-T-G

13571776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211461-G-A

13571776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211461-G-T

13571992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211653-C-G

13571992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91211653-C-T

13574129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213918-G-A

13574783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213382-C-T

13574833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213335-G-C

13574835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213333-G-A

13574868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213298-G-A

13574898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91213269-C-T

13574964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213221-T-C

13575037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213153-G-A

13575037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213153-G-C

13575110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91213080-G-T

13575191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91212997-C-T

13575232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91212956-G-A

13575269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91212939-A-G

13575463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91212813-T-C

13575711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91212611-G-C

13575775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91212549-C-T

13575787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91212537-C-G

13582757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91217469-C-T

13582953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91217656-T-A

13583101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91217789-C-T

13583334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91217996-A-G

13583355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218016-C-T

13583507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218166-G-A

13583747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218337-G-C

13584122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218676-C-T

13584135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218685-T-C

13584379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218926-G-C

13584379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91218926-G-T

13584434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219006-C-T

13584573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219144-G-C

http://identifiers.org/hco/3/GRCh38#13584627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91219171-C-A

13584640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219184-C-T

13584648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219192-C-T

13584681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219229-G-A

13584683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219231-G-A

13584889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91219426-T-C

13595472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222322-C-T

13595491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222339-G-C

13595531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222388-C-T

13595632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222479-G-T

13595724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222569-A-G

13595754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222597-T-C

13596070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91222871-A-G

13598737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224130-A-G

13599141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224531-C-T

13599172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224576-G-A

13599416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224817-T-G

13599428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224845-T-C

13599474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91224891-C-T

http://identifiers.org/hco/3/GRCh38#13599608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91225022-C-A

13599635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91225049-G-T

13599669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91225083-G-T

13599756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, undefined
orthologous variants: 91225134-C-T

13600330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91225566-C-T

13600402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91225658-G-A

13607654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227400-G-A

13607793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227543-G-T

13607985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227763-A-T

13608018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227796-G-A

13608018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227796-G-T

http://identifiers.org/hco/3/GRCh38#13608076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91227854-C-A

13608076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91227854-C-G

13608105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91227883-G-A

13608145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91227923-G-A

13608145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: stop gained
orthologous variants: 91227923-G-T

http://identifiers.org/hco/3/GRCh38#13608188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91227961-C-A

13608188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91227961-C-G

13608915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228801-C-G

13608919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228805-T-C

13609019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228904-G-A

13609019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228904-G-T

13609039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228938-T-C

13609039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228938-T-G

13609065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228973-C-G

13609065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91228973-C-T

13609133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229052-C-T

13609185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229105-T-C

13609191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229109-C-G

13609248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229167-G-T

13609255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229170-A-G

13609267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229183-A-G

http://identifiers.org/hco/3/GRCh38#13609348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229237-A-C

http://identifiers.org/hco/3/GRCh38#13609381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229270-C-A

13609381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229270-C-T

http://identifiers.org/hco/3/GRCh38#13609384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229273-C-A

13609384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229273-C-T

http://identifiers.org/hco/3/GRCh38#13609392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229281-C-A

13609392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229281-C-T

http://identifiers.org/hco/3/GRCh38#13609396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229285-C-A

13609396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229285-C-T

http://identifiers.org/hco/3/GRCh38#13609402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229291-C-A

13609402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229291-C-T

13609403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229292-T-C

http://identifiers.org/hco/3/GRCh38#13609410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229300-C-A

13609410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229300-C-T

http://identifiers.org/hco/3/GRCh38#13609418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229308-C-A

13609419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229309-T-A

13609419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229309-T-C

http://identifiers.org/hco/3/GRCh38#13609462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229353-C-A

13609474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229383-G-A

13609510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91229423-C-T

http://identifiers.org/hco/3/GRCh38#13609570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229483-C-A

13609570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91229483-C-T

13609579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91229492-A-G

http://identifiers.org/hco/3/GRCh38#13609621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229534-C-A

13609621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91229534-C-G

13609621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91229534-C-T

http://identifiers.org/hco/3/GRCh38#13609654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229567-C-A

13609654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229567-C-G

13609654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229567-C-T

http://identifiers.org/hco/3/GRCh38#13609752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91229601-C-A

13609752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91229601-C-T

13613216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91230684-T-A

13613243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91230712-C-G

13613476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91230922-T-C

13613476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91230922-T-G

13613825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91231237-G-T

13613936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91231325-C-G

13614037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91231476-G-A

13614037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91231476-G-C

13614037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91231476-G-T

http://identifiers.org/hco/3/GRCh38#13614145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91231584-C-A

13614145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91231584-C-T

13614174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231613-G-A

13614174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231613-G-T

13614286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231744-G-A

13614286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231744-G-T

http://identifiers.org/hco/3/GRCh38#13614297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91231755-A-C

13614297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231755-A-G

13614466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231919-G-T

13614498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91231934-C-T

http://identifiers.org/hco/3/GRCh38#13614625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91232031-C-A

13614625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232031-C-T

13614634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232038-T-A

13614634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232038-T-C

13614634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232038-T-G

13614727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232136-C-T

13616254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232244-T-A

13616549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232662-A-G

13616550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232663-C-T

13616799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232775-C-T

13616829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232808-G-A

13616852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232831-C-T

13616891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232857-A-G

13616904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232869-G-A

13616916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232882-G-C

13616916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232882-G-T

13616922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232888-A-G

13616942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91232907-C-T

13617868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233036-A-G

13617906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233073-C-T

http://identifiers.org/hco/3/GRCh38#13617953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91233117-C-A

13617953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233117-C-T

http://identifiers.org/hco/3/GRCh38#13618024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91233166-C-A

13618042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233182-C-T

13618085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91233226-C-T

13618149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91233290-G-A

http://identifiers.org/hco/3/GRCh38#13618754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91233715-C-A

13618754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233715-C-T

13618802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233774-G-A

13618802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233774-G-C

13618802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233774-G-T

http://identifiers.org/hco/3/GRCh38#13618853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91233816-C-A

13618853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233816-C-G

http://identifiers.org/hco/3/GRCh38#13618889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91233847-C-A

13618889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233847-C-G

13618889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91233847-C-T

13619031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91233988-G-A

13619031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91233988-G-T

13619083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234034-G-A

13619083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234034-G-C

13619083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234034-G-T

http://identifiers.org/hco/3/GRCh38#13619124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91234074-C-A

13619124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234074-C-T

13619184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234221-A-T

13619204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234241-A-G

13619213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234250-G-A

13619526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234522-G-A

13619535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234531-C-T

13619610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234603-G-A

13619788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91234765-T-C

13619895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234871-A-G

13619895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234871-A-T

http://identifiers.org/hco/3/GRCh38#13619924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91234900-C-A

13619931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91234907-T-C

13620047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235000-T-C

13620047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235000-T-G

13620103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235034-G-A

13620110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235042-G-A

13620401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235381-G-A

13620452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235434-A-T

13620537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235502-G-A

13620666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235619-G-A

13620790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235733-C-T

13620837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235776-G-A

http://identifiers.org/hco/3/GRCh38#13621054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91235961-C-A

13621057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91235964-C-T

13621251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236117-C-T

13621451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236307-G-A

13621514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236373-T-C

13621708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236548-G-A

13621936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236774-C-T

13621945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236785-G-A

13621945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236785-G-C

13621945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236785-G-T

http://identifiers.org/hco/3/GRCh38#13621956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91236796-C-A

13622028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236869-T-A

13622073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91236911-C-T

http://identifiers.org/hco/3/GRCh38#13622258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91237059-C-A

13622258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91237059-C-T

13622410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91237175-C-T

13622632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91237368-A-G

13622760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91237495-G-A

13623355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238052-C-T

13623840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238379-T-C

13623887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238395-A-G

13624074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238514-C-T

http://identifiers.org/hco/3/GRCh38#13624175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91238599-A-C

13624245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238655-G-A

13624307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238737-C-G

13624336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238767-G-A

13624336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238767-G-T

13624352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238787-C-G

13624599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91238969-T-A

13624674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239044-G-A

13624674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239044-G-C

http://identifiers.org/hco/3/GRCh38#13624713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91239082-C-A

13624713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239082-C-T

13625495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239453-C-T

13625537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239502-A-G

13625537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239502-A-T

13625542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239505-C-T

13625651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239608-G-A

13625651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239608-G-T

13625652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239609-T-C

13625987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239884-C-T

13625988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239885-A-G

13625988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239885-A-T

13626072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91239970-G-A

13626258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240125-G-A

13626382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240259-T-A

13626393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240270-A-G

13626393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240270-A-T

13626408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240281-G-A

13626408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240281-G-T

13626506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91240382-A-G

13626610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240483-G-A

13626637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240541-G-A

13626637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240541-G-C

13626637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240541-G-T

13626680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240603-G-A

http://identifiers.org/hco/3/GRCh38#13626693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91240616-C-A

13626693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240616-C-T

13626706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240629-C-G

13626706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240629-C-T

13626707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240630-T-A

13626707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240630-T-C

13626709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240632-C-T

13626811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240721-G-T

13626888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240794-A-G

13626975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91240880-A-G

13627122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241011-C-T

13627636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241455-C-T

http://identifiers.org/hco/3/GRCh38#13627697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91241513-C-A

13627697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241513-C-T

13627708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241524-T-C

http://identifiers.org/hco/3/GRCh38#13627720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91241539-C-A

http://identifiers.org/hco/3/GRCh38#13627729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91241552-C-A

13627729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241552-C-T

13627778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241625-G-A

13627785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241632-G-A

13627785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241632-G-T

13628094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241909-T-C

http://identifiers.org/hco/3/GRCh38#13628098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91241913-C-A

13628098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241913-C-T

13628113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241929-G-A

13628113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91241929-G-T

13628368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242091-G-C

13628564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242264-C-T

13628748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242595-G-T

13628795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242642-G-A

13628795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242642-G-T

13628800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242647-G-A

13628800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242647-G-T

http://identifiers.org/hco/3/GRCh38#13628872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91242669-C-A

13628872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242669-C-G

13628872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242669-C-T

13628943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91242738-C-T

13629006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91242801-G-A

13629006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91242801-G-C

13629061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242855-G-A

13629061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242855-G-T

13629138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91242910-C-T

13629194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91242968-G-A

13629194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91242968-G-T

13629255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91243029-C-T

13629306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243081-T-A

13629307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243082-G-A

13629307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243082-G-T

http://identifiers.org/hco/3/GRCh38#13629329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243104-C-A

13629329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243104-C-T

13629379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243123-T-A

13629379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243123-T-C

http://identifiers.org/hco/3/GRCh38#13629439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243172-A-C

13629439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243172-A-G

http://identifiers.org/hco/3/GRCh38#13629462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243188-A-C

13629462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243188-A-G

http://identifiers.org/hco/3/GRCh38#13629718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243246-C-A

13629718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243246-C-T

13629827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91243304-T-C

13629827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91243304-T-G

http://identifiers.org/hco/3/GRCh38#13629881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243358-C-A

13629881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91243358-C-T

13629902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91243379-C-T

13629949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243427-G-A

13629960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243438-A-G

http://identifiers.org/hco/3/GRCh38#13629969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91243447-C-A

13629969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243447-C-T

13630304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243789-A-G

13630320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243805-G-A

13630434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91243914-A-G

http://identifiers.org/hco/3/GRCh38#13630754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245575-C-A

13630754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91245575-C-T

http://identifiers.org/hco/3/GRCh38#13630825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245648-C-A

13630825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245648-C-T

13630837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245653-G-A

13630837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245653-G-T

http://identifiers.org/hco/3/GRCh38#13630856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245672-C-A

13630856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245672-C-G

13630856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245672-C-T

http://identifiers.org/hco/3/GRCh38#13630858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245674-C-A

http://identifiers.org/hco/3/GRCh38#13630872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245688-C-A

http://identifiers.org/hco/3/GRCh38#13630952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245738-A-C

13630952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245738-A-G

http://identifiers.org/hco/3/GRCh38#13631181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245960-C-A

13631181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245960-C-T

13631185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245964-T-C

http://identifiers.org/hco/3/GRCh38#13631188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91245967-C-A

13631188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245967-C-T

13631202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245981-G-A

13631202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91245981-G-T

http://identifiers.org/hco/3/GRCh38#13631231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246008-C-A

13631231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246008-C-G

13631231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246008-C-T

13631297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246043-G-T

http://identifiers.org/hco/3/GRCh38#13631333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246074-C-A

13631333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246074-C-T

13631408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246149-A-G

13631420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246161-G-A

13631420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: missense variant
orthologous variants: 91246161-G-T

http://identifiers.org/hco/3/GRCh38#13631426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246167-C-A

13631426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246167-C-T

http://identifiers.org/hco/3/GRCh38#13631482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246219-C-A

13631482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246219-C-T

13631506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246255-G-T

http://identifiers.org/hco/3/GRCh38#13631511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246260-C-A

13631511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246260-C-G

13631511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246260-C-T

13631544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246280-T-C

13631579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246303-A-G

13631772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246452-C-T

13636124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246596-C-T

13636323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246819-G-A

http://identifiers.org/hco/3/GRCh38#13636363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246861-C-A

13636432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91246930-T-C

http://identifiers.org/hco/3/GRCh38#13636470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91246971-C-A

13636470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246971-C-G

13636470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: synonymous variant
orthologous variants: 91246971-C-T

13636584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91247085-C-T

13637116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248125-C-T

13637183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248176-G-C

13637264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248232-G-A

13637294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248247-C-T

13637415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248346-G-T

13637419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248349-G-A

13637419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248349-G-C

13637419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248349-G-T

13637473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248403-T-A

http://identifiers.org/hco/3/GRCh38#13637474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91248404-C-A

13637474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248404-C-G

13637474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248404-C-T

http://identifiers.org/hco/3/GRCh38#13637492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91248427-C-A

13637492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248427-C-T

http://identifiers.org/hco/3/GRCh38#13637502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91248445-C-A

13637502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248445-C-G

13637510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248454-G-T

13637515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248455-G-A

13637515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248455-G-T

13637539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248481-G-A

13637539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron variant
orthologous variants: 91248481-G-T

http://identifiers.org/hco/3/GRCh38#13637555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91248497-C-A

13637555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91248497-C-G

http://identifiers.org/hco/3/GRCh38#13637574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_donor_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91248516-C-A

13637574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, splice_donor_variant, synonymous_variant
orthologous variants: 91248516-C-T

13637625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 91248567-G-A

13637625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 91248567-G-C

13637938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91248882-C-G

13637938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91248882-C-T

13638142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 91249034-G-A

13638142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 91249034-G-T

http://identifiers.org/hco/3/GRCh38#13638143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91249035-C-A

13638143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 91249035-C-T

13638170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 91249046-T-A

13638170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 91249046-T-C

13638170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 91249046-T-G

13638177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 91249053-G-A

13638177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 91249053-G-T

http://identifiers.org/hco/3/GRCh38#13638185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91249061-A-C

13638185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 91249061-A-G

13638185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 91249061-A-T

http://identifiers.org/hco/3/GRCh38#13638210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91249082-A-C

13638210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 91249082-A-G

13638210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3601
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 91249082-A-T