61943213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86158527-G-A

61943279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86158593-A-T

61944082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86159375-G-A

61944082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86159375-G-T

61944411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86159713-T-A

61944411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86159713-T-C

61945236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86160525-C-T

http://identifiers.org/hco/17/GRCh38#61946247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86161600-C-A

61946247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86161600-C-G

61946247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: 3 prime UTR variant
orthologous variants: 86161600-C-T

61946885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163257-G-A

61946885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163257-G-T

61947364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163564-G-C

61947404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163606-C-T

61947531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163731-A-G

61947531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163731-A-T

61947741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86163969-A-G

61949146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86165233-G-A

61949166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86165252-T-C

61949430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86165545-T-C

http://identifiers.org/hco/17/GRCh38#61950735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86166109-C-A

61950735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86166109-C-G

61950735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86166109-C-T

61950808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86166183-G-A

http://identifiers.org/hco/17/GRCh38#61951094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86166459-C-A

61952653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86167549-C-G

61953116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 86167797-A-G

61954201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86168790-G-A

http://identifiers.org/hco/17/GRCh38#61954233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86169032-A-C

61954237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86169036-T-C

61954248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86169047-G-A

61956004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86169891-C-T

61957727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86171472-G-T

61960801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86173949-T-C

61960801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86173949-T-G

61960819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86173963-A-G

61961111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174270-G-C

61961111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174270-G-T

http://identifiers.org/hco/17/GRCh38#61961564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86174552-C-A

61961564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174552-C-G

61961564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174552-C-T

61961830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174821-A-G

61961843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174829-G-A

61961843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174829-G-T

http://identifiers.org/hco/17/GRCh38#61961878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86174844-A-C

61961878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86174844-A-G

61962666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86175717-T-C

61962689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86175739-G-T

http://identifiers.org/hco/17/GRCh38#61962703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86175770-C-A

61962723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86175798-T-C

61962755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86175942-T-A

61962884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86176071-A-G

61964072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86176830-T-C

61964080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86176838-G-C

61964268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86177049-T-C

61965092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86177346-C-T

61965289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: missense variant
orthologous variants: 86177537-C-T

http://identifiers.org/hco/17/GRCh38#61965594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86177828-C-A

61965594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86177828-C-T

61965612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86177849-T-C

http://identifiers.org/hco/17/GRCh38#61965727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86177971-A-C

61965727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86177971-A-G

61966039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86178399-A-G

61966267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86178724-A-G

61966417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86178874-C-T

61966673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179127-G-A

61966673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179127-G-C

61966673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179127-G-T

61966696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179150-G-A

61966696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179150-G-T

61966748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179206-T-A

61966748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179206-T-C

61967949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179701-A-G

61967969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86179721-T-G

61968263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 86179987-A-G

61972411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86181590-A-T

61972475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86181642-A-G

61972591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86181754-T-C

61973036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86182172-A-G

61983220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86190124-A-G

http://identifiers.org/hco/17/GRCh38#61983242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86190146-C-A

61983593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86190841-T-C

61983613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86190881-T-C

61983632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86190899-A-G

61984385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191690-T-C

61984579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191892-G-A

61984579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191892-G-C

61984579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191892-G-T

61984598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191907-T-C

61984602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191911-A-G

61984637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86191946-A-G

61984828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86192133-T-C

61984944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192236-T-C

61984968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192259-A-G

61985174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192459-G-T

61985211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192496-T-A

61985228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192514-T-A

61985228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192514-T-C

61985336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86192606-T-C

61986320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86193333-G-T

61986427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86193434-G-A

61986586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86193803-G-C

61986812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86194170-G-A

61986817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86194175-T-G

http://identifiers.org/hco/17/GRCh38#61986940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86194294-A-C

61986940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86194294-A-G

61987112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86194465-A-G

61989767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86196042-G-A

61989859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86196086-G-A

61989884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86196111-T-A

61990003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86196241-A-G

61992454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86197614-G-A

61992454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86197614-G-T

61992520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86197708-T-C

61992594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: missense variant
orthologous variants: 86197861-C-G

http://identifiers.org/hco/17/GRCh38#61992703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86197969-C-A

61993012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86198261-A-G

61993012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86198261-A-T

61993165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86198444-A-G

61993175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86198454-G-C

61993175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86198454-G-T

61995176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86199549-C-T

61995376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86199753-A-G

http://identifiers.org/hco/17/GRCh38#61996014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86200301-A-C

61996321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86200609-G-A

61996321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86200609-G-C

61997180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86201480-C-T

61997182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86201482-T-C

61997419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86201700-G-C

61997496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86201777-C-T

61997641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86201903-G-C

61998952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86202824-C-T

61998973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86202844-A-G

61998973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86202844-A-T

61999061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86202907-T-C

61999599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86203569-C-G

61999782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86203767-T-C

61999790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86203775-C-T

http://identifiers.org/hco/17/GRCh38#61999858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86203851-A-C

61999867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86203860-G-C

62002751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86205194-G-A

http://identifiers.org/hco/17/GRCh38#62003812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86206487-C-A

62003916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86206588-G-A

62003994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86206626-T-G

62004230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86206886-G-A

62004320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86206974-T-C

62004373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86207029-G-T

62004446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86207099-A-T

62009280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86209270-T-A

62010289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86209922-T-A

62010289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86209922-T-C

62011286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86210918-G-A

62011286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86210918-G-T

62011351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86210977-A-G

62011557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86211345-T-C

62017579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86213519-T-G

62017603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86213539-G-A

62017603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86213539-G-T

62017867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86213895-C-T

62025364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86217084-A-G

62026324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86218078-T-G

62026421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86218145-C-G

http://identifiers.org/hco/17/GRCh38#62029391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86218495-C-A

http://identifiers.org/hco/17/GRCh38#62029398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86218502-C-A

62029398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86218502-C-T

62029686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86218809-A-G

62029952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86219374-G-A

62030120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219536-G-T

62030139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219555-G-A

62030139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219555-G-T

62031143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219715-G-A

62031143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219715-G-T

62031193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219764-G-T

62031195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219766-T-C

62031195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219766-T-G

62031201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219772-A-G

62031226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219797-T-C

62031389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86219929-T-C

62031704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86220270-A-G

62033236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221289-T-C

62033593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221639-G-A

62033614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221660-T-C

62033646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221692-G-A

62033646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221692-G-T

62033697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221743-A-G

62033697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221743-A-T

62033709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86221750-T-C

62033836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86221863-T-C

62034097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86222108-A-G

http://identifiers.org/hco/17/GRCh38#62034486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86222225-C-A

62034486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86222225-C-T

62035621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86222867-A-G

62036536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86223588-T-C

62036871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86224066-T-A

http://identifiers.org/hco/17/GRCh38#62036872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86224067-C-A

62036872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86224067-C-G

62036934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86224123-G-A

62036934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86224123-G-T

http://identifiers.org/hco/17/GRCh38#62038917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86227871-C-A

62038982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86227934-T-C

62039053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86228003-G-T

62040107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86228262-C-G

62040297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86228449-G-A

62041184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86230044-G-A

62041430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86230499-T-A

62041814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86230812-C-T

62042037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86231022-G-C

62042267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86231339-T-C

62044210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86233186-C-T

62044336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86233291-T-C

62045625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86234828-A-G

http://identifiers.org/hco/17/GRCh38#62045811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86235020-C-A

62045811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86235020-C-T

62045888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86235094-T-G

http://identifiers.org/hco/17/GRCh38#62052532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86236681-C-A

62052532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86236681-C-T

62052635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: synonymous variant
orthologous variants: 86236784-G-A

62052635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: missense variant
orthologous variants: 86236784-G-T

62052985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86237306-G-A

62053147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86237472-C-T

http://identifiers.org/hco/17/GRCh38#62053553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86237822-C-A

62053942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86238468-T-C

62054581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86238738-G-T

62054699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86238842-T-C

http://identifiers.org/hco/17/GRCh38#62055995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86239898-A-C

62055995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86239898-A-G

62056021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86239924-G-A

62056063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86239966-G-A

62056789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86240373-T-C

62057028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86240618-A-G

62057305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86240916-C-G

62057621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86241186-C-T

62057714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86241274-C-G

62057916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86241467-C-G

62057916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86241467-C-T

62058084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86241573-C-T

62059111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86242215-A-T

62059386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86242596-A-G

62059995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86243207-T-G

62061488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86243707-T-C

62061790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86244193-A-T

62061942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86244446-T-C

62061951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86244455-G-A

62062304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86245397-G-A

62062366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86245456-G-T

62062466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86245558-T-C

62062469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86245561-T-C

62062505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86245614-A-G

http://identifiers.org/hco/17/GRCh38#62062968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86246022-C-A

62062968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86246022-C-T

62063393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86246488-A-G

http://identifiers.org/hco/17/GRCh38#62063437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86246549-C-A

62063980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86247106-G-C

62064761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86247873-G-A

62064761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86247873-G-C

62064860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86247983-T-A

62064871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86247994-G-A

62064958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22474
most severe consequence: intron variant
orthologous variants: 86248106-G-A