61808307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204878-G-A

61808307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204878-G-C

61808307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204878-G-T

http://identifiers.org/hco/18/GRCh38#61808352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105204923-C-A

61808415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204972-T-A

61808415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204972-T-C

61808415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204972-T-G

61808423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204980-T-A

61808423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204980-T-C

61808430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204987-T-A

61808430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105204987-T-C

http://identifiers.org/hco/18/GRCh38#61808475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105205032-C-A

61808608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205167-C-G

61808640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205199-T-C

http://identifiers.org/hco/18/GRCh38#61808700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105205262-C-A

61808700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205262-C-T

61808764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205320-G-T

61808784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205340-G-A

61808852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205406-G-A

61808852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205406-G-C

61808852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205406-G-T

61808995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105205532-G-T

61809538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206009-G-A

61809631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206106-A-G

61809659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206135-A-G

61809734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206204-T-C

61809828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206296-T-A

61809828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206296-T-C

61809847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206315-G-T

61809887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206345-T-A

61809887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206345-T-C

61809977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206436-G-C

61810045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105206633-G-A

61810798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207039-G-C

61810865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207106-G-T

61810972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207208-G-A

61810972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207208-G-T

61811000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207236-T-C

http://identifiers.org/hco/18/GRCh38#61811097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105207310-C-A

61811378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207599-T-C

61811647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207858-T-C

61811668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207879-T-C

61811723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105207933-A-G

61811827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208056-G-A

http://identifiers.org/hco/18/GRCh38#61811926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105208155-C-A

http://identifiers.org/hco/18/GRCh38#61812039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105208272-C-A

61812039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208272-C-T

61812125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208307-G-T

61812363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208524-C-T

61812461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208625-G-T

61812674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208837-A-G

http://identifiers.org/hco/18/GRCh38#61812788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105208945-C-A

61812791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105208948-T-C

http://identifiers.org/hco/18/GRCh38#61812853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105209005-C-A

61812917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209062-G-C

61812950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209095-G-C

61812964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209109-G-T

http://identifiers.org/hco/18/GRCh38#61812976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105209121-C-A

61812976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209121-C-T

61812979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209124-A-G

61812986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209131-A-G

http://identifiers.org/hco/18/GRCh38#61813036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105209207-C-A

61813044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209215-G-T

61813597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209689-A-G

61813877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209958-C-T

61813878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105209959-A-G

61814050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210133-C-T

61814144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210227-A-G

http://identifiers.org/hco/18/GRCh38#61814316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105210389-C-A

61814316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210389-C-G

61814316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210389-C-T

61814583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210628-T-C

61814583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210628-T-G

http://identifiers.org/hco/18/GRCh38#61814630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105210670-C-A

61814630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210670-C-T

61814688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210728-T-C

61814921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105210961-C-T

61815133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211170-G-C

http://identifiers.org/hco/18/GRCh38#61815170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105211208-C-A

61815170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211208-C-G

61815170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211208-C-T

http://identifiers.org/hco/18/GRCh38#61815204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105211242-C-A

61815270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211309-T-C

61815275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211314-A-T

61815308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211347-G-T

61815437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211541-G-A

61815437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211541-G-T

http://identifiers.org/hco/18/GRCh38#61815463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105211566-C-A

http://identifiers.org/hco/18/GRCh38#61815653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105211752-C-A

61815653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211752-C-T

http://identifiers.org/hco/18/GRCh38#61815697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105211796-C-A

61815697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211796-C-T

61815758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211849-G-T

61815787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 3 prime UTR variant
orthologous variants: 105211877-G-T

61816071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: synonymous variant
orthologous variants: 105212163-G-A

61816097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: missense variant
orthologous variants: 105212189-G-A

61816101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: synonymous variant
orthologous variants: 105212193-C-T

61816122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: synonymous variant
orthologous variants: 105212214-G-A

61816470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105212562-C-T

61816490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105212581-G-T

61816588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105212669-T-G

61816652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212738-G-T

61816681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212762-G-A

61816701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212782-G-T

61816740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212824-G-T

61816752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212836-G-A

61817050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212896-G-A

61817068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105212914-C-T

61817788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105213936-G-A

61817834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105213982-G-A

61817913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214061-C-G

61817913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214061-C-T

http://identifiers.org/hco/18/GRCh38#61818148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105214213-C-A

61818148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214213-C-T

61818149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214214-G-A

61818151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214216-G-C

61818163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214219-C-T

http://identifiers.org/hco/18/GRCh38#61818438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105214414-C-A

http://identifiers.org/hco/18/GRCh38#61818439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105214415-A-C

61818738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214806-A-G

61818747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214816-G-A

61818848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214905-A-G

61818934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105214981-G-T

http://identifiers.org/hco/18/GRCh38#61818998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105215045-C-A

61819019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105215072-C-T

61819298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105215469-C-T

61819334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105215505-G-C

61819434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105215592-C-T

61820554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105217363-C-T

http://identifiers.org/hco/18/GRCh38#61820909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105217681-C-A

61821211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105217926-T-C

61821212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105217927-G-C

61821456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105218198-G-T

61822081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105218470-G-A

61822081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105218470-G-T

61822171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105218563-C-T

61822501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105218825-A-T

61822776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105219082-G-A

http://identifiers.org/hco/18/GRCh38#61823065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105219352-C-A

61823648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105219623-G-A

61823938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105219891-G-T

61824044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105220178-G-C

61824101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105220229-C-T

61824163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105220286-G-T

61824342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105220426-A-G

61824626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221019-G-C

61824792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221203-A-G

61824940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221348-C-G

61824940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221348-C-T

61824965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221356-A-G

61825156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221541-T-G

61825186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221578-G-A

61825406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105221765-A-T

61825579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, undefined
orthologous variants: 105221859-A-G

http://identifiers.org/hco/18/GRCh38#61825788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105222072-C-A

61825788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105222072-C-T

61826127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105222556-A-G

61826136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105222565-G-A

http://identifiers.org/hco/18/GRCh38#61826295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105222719-A-C

61826857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105223565-G-A

61827588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105225287-G-C

61827588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105225287-G-T

61828991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105226603-T-C

61828997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105226608-T-C

61830951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105226779-C-G

61830995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105226823-T-A

http://identifiers.org/hco/18/GRCh38#61831099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105226929-A-C

61831107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105226938-G-A

61831906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227673-T-A

61831946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227697-G-A

http://identifiers.org/hco/18/GRCh38#61831969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105227716-A-C

61832161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227840-G-A

61832210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227876-T-C

61832291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227953-A-G

61832316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105227980-G-A

61832578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105228303-A-G

61832714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105228750-A-G

61832714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105228750-A-T

61832889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105228912-C-T

61833236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105229360-T-G

61833247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105229371-A-T

61833487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105229605-T-G

61833505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, undefined
orthologous variants: 105229621-C-G

61833689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, undefined
orthologous variants: 105229780-G-C

61833799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105229879-A-G

61833851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105229919-G-C

61833953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105230011-T-A

61833953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105230011-T-G

61833954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105230012-G-A

61837389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105231085-T-G

61838656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105232226-C-T

61838746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105232316-C-T

61839222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105232779-T-A

61839382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105232909-G-A

61839552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105233046-C-T

61839878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105233431-T-A

61840005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105233540-G-A

61840005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105233540-G-C

61840056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105233586-A-G

61840280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105237685-C-G

61840345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105237746-G-A

61840349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105237750-T-C

61840393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105237789-A-G

61840611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105238054-G-A

61840925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105238329-T-C

61841039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238420-G-A

61841039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238420-G-T

61841093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238472-T-C

61841252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238616-G-A

61841537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238841-T-C

61841578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238880-C-T

61841583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238888-G-C

61841585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105238890-G-A

61841947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105239236-C-T

61842396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105240185-C-T

61842469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105240256-C-T

61842553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105240323-G-C

61842561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105240331-G-A

61844587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105241965-T-A

61844587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105241965-T-C

61844679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242039-C-G

61844742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242079-C-T

61844853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242179-G-A

61844853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242179-G-C

61844853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242179-G-T

61845675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242655-A-G

61845838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242770-G-A

61846006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242870-G-A

61846016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242887-G-A

61846046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105242921-C-T

61846506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243306-T-A

61846506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243306-T-G

61846546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243344-C-T

61846565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243371-C-T

61846636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243412-G-A

61846664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243439-G-A

61846855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105243583-A-G

61847271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105244833-G-A

61847330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105244890-C-T

61847331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105244891-G-A

61847345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105244903-A-T

61847716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105245316-G-A

61848503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105246863-C-T

61848526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105246880-C-T

61848702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105247039-G-A

http://identifiers.org/hco/18/GRCh38#61848710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105247047-C-A

61848783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105247110-G-C

61848891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 105247241-G-A

61851608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105249595-G-A

http://identifiers.org/hco/18/GRCh38#61851664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105249647-C-A

61851826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105249800-T-C

61852010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, undefined
orthologous variants: 105249975-C-T

http://identifiers.org/hco/18/GRCh38#61853108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105251010-C-A

61853191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105251084-G-T

http://identifiers.org/hco/18/GRCh38#61854039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105251935-C-A

61854062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105251958-A-T

61854105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252004-C-T

61854212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252101-G-A

61854293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252202-C-G

61854293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252202-C-T

61854494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252378-A-T

http://identifiers.org/hco/18/GRCh38#61854528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105252412-C-A

61854528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252412-C-T

61854551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252431-G-A

61854558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252438-A-T

61854778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252541-G-A

61854914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252660-T-A

http://identifiers.org/hco/18/GRCh38#61854943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105252689-C-A

61855030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105252762-T-C

61856871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105253365-A-G

61857140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105253610-C-T

http://identifiers.org/hco/18/GRCh38#61857252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105253722-A-C

http://identifiers.org/hco/18/GRCh38#61857434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105254440-C-A

61857665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105254712-T-G

http://identifiers.org/hco/18/GRCh38#61857875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105254877-A-C

61858194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255187-T-C

61858194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255187-T-G

61858476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255364-C-T

61858631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255526-C-T

61858632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255527-G-A

61858832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105255815-A-G

61859082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256074-A-T

61859224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256216-A-T

61859998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256615-G-A

61860138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256761-G-A

61860139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256762-G-A

61860194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105256799-C-G

61864242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258235-G-A

61864412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258363-C-T

61864585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258535-G-A

http://identifiers.org/hco/18/GRCh38#61864925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105258855-C-A

61864925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258855-C-T

61864947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258869-G-A

http://identifiers.org/hco/18/GRCh38#61864984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105258904-C-A

61865027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258938-A-G

61865027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105258938-A-T

61865712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105259698-C-T

61865775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105259746-G-A

61866006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105259957-A-G

61866019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105259968-G-A

61866044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105259995-T-C

61866059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260011-C-T

61866084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260032-C-T

http://identifiers.org/hco/18/GRCh38#61866173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105260093-C-A

61866219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260136-T-C

61866455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260290-C-G

61866474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260309-T-C

61867807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260374-T-A

61867839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260411-C-T

61867852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260424-T-C

61867898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260469-C-T

61867903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260474-C-T

61868409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105260836-G-A

61869281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105261651-G-C

61869281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105261651-G-T

61869407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105261778-G-A

61869407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105261778-G-T

61869461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105261828-G-A

http://identifiers.org/hco/18/GRCh38#61869913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105262121-A-C

61869945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262152-T-A

61870014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262457-A-G

61870042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262497-A-G

61870086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262539-C-T

61870146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262596-C-T

61870176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262626-T-C

61870239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262675-T-C

61870389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105262818-G-A

61871397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105263552-A-T

61871725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264057-G-C

61871773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264103-G-C

61872433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264332-A-G

61872549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264447-C-T

61872726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264605-T-A

61872726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105264605-T-C

61873163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105266150-C-T

61873237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105266225-T-C

61873746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105266726-G-A

61873746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105266726-G-T

61874436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105266997-C-T

http://identifiers.org/hco/18/GRCh38#61874969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105267183-C-A

http://identifiers.org/hco/18/GRCh38#61874981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105267196-C-A

http://identifiers.org/hco/18/GRCh38#61874992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105267207-C-A

61874992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105267207-C-T

61875004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105267223-T-A

61875004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron variant
orthologous variants: 105267223-T-C

61875164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267364-T-C

61875199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267399-G-A

61875229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267429-G-C

61875231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267431-A-G

61875323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267521-C-T

http://identifiers.org/hco/18/GRCh38#61875431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105267640-C-A

61875431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267640-C-G

61875646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267869-T-A

61875646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267869-T-C

61875776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267989-G-A

61875776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267989-G-T

61876009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105268196-C-T

61876718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105268570-T-C

61877810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105269607-C-G

61877810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105269607-C-T

61877903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105269707-T-C

http://identifiers.org/hco/18/GRCh38#61877928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105269732-A-C

61878314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105270103-G-C

61878456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105270227-A-G

61880113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105270706-C-T

61880638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105271512-T-A

61880723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105271594-T-C

61881581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272242-T-A

61881612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272273-C-T

61881756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272323-C-T

61881768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272336-G-A

61881768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272336-G-T

61881854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272426-A-T

61881873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272445-A-G

61882790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105273035-T-C

61882806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105273051-C-G

61882806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105273051-C-T

61883408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273682-T-C

61884204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275210-A-G

http://identifiers.org/hco/18/GRCh38#61884300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105275286-C-A

61884425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275396-C-T

61884523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275474-G-A

http://identifiers.org/hco/18/GRCh38#61884870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105275507-A-C

61884900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275537-G-A

61885587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276407-C-T

61885588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276408-G-A

61885668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276493-T-C

61885756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276553-T-A

61885756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276553-T-C

61885887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276650-G-A

61885887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276650-G-T

61886117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276816-T-C

61886354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277033-A-G

61886358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277037-C-T

61886364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277043-G-T

61886480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277083-G-A

61887075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277606-A-G

61887075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277606-A-T

61887331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277835-A-G

61887408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105277960-G-A

61887518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278051-A-G

61887668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278182-C-G

61887668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278182-C-T

61887843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278351-C-T

http://identifiers.org/hco/18/GRCh38#61887922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278392-C-A

61887922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278392-C-G

http://identifiers.org/hco/18/GRCh38#61887924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278394-C-A

61887933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278403-G-A

61887933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278403-G-T

61887942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278418-G-T

61887949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278425-C-T

http://identifiers.org/hco/18/GRCh38#61887968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278440-C-A

61888038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278494-T-A

http://identifiers.org/hco/18/GRCh38#61888161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278633-C-A

http://identifiers.org/hco/18/GRCh38#61888166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278638-C-A

http://identifiers.org/hco/18/GRCh38#61888171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278643-C-A

61888171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278643-C-G

61888171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278643-C-T

61888179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278650-G-A

61888179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278650-G-T

61888197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278669-G-A

61888271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278730-A-G

http://identifiers.org/hco/18/GRCh38#61888804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105278804-C-A

61888804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105278804-C-T

61888916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278917-G-A

61888916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278917-G-T

61888917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278918-A-G

61889007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278990-G-T

61889235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105279162-G-A

61889414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105279306-A-T

61889571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105279451-C-T

61890202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105280399-G-C

http://identifiers.org/hco/18/GRCh38#61890488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105280630-C-A

61890488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280630-C-T

61890492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280634-G-T

61890529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105280657-T-C

61891118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105281202-C-T

61891263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105281311-A-T

61891265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105281313-A-G

61891463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105281520-T-C

61891795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105281847-T-C

61892343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282308-C-G

61892343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282308-C-T

61892383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282348-G-A

61892624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282559-A-T

61892783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282755-G-A

61892783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282755-G-C

61892783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282755-G-T

61892808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105282778-C-T

61892859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105282830-G-A

61892859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105282830-G-T

61893004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105282975-G-A

61893004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105282975-G-C

61893004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105282975-G-T

61893020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282991-T-C

61893039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283002-T-A

61893039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283002-T-C

61893057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283021-G-A

61893057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283021-G-T

61893193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283154-A-G

61893319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283302-C-T

http://identifiers.org/hco/18/GRCh38#61893324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105283307-C-A

61893671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105283620-A-G

61893723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105283670-G-A

61893723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105283670-G-C

61893760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105283707-A-G

61893835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283781-G-A

61893835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283781-G-T

61893889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283833-G-A

http://identifiers.org/hco/18/GRCh38#61893910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105283853-C-A

http://identifiers.org/hco/18/GRCh38#61893982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105283918-C-A

61893982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283918-C-G

61893982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283918-C-T

61893984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283920-T-C

61894014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283952-G-A

61894014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283952-G-T

61894020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283958-G-A

http://identifiers.org/hco/18/GRCh38#61894088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105284007-C-A

61894088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284007-C-T

61894089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284008-C-T

http://identifiers.org/hco/18/GRCh38#61894119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105284037-A-C

http://identifiers.org/hco/18/GRCh38#61894168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105284086-C-A

61894168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105284086-C-G

61894168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105284086-C-T

http://identifiers.org/hco/18/GRCh38#61894187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105284103-C-A

61894187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105284103-C-T

61894222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105284140-G-A

61894293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105284213-G-A

61894293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105284213-G-C

61894407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26811
most severe consequence: 5 prime UTR variant
orthologous variants: 105284337-C-T