107163634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251566-G-A

107163678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251611-T-C

107163765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251693-T-G

http://identifiers.org/hco/13/GRCh38#107163955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9251882-C-A

107163955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251882-C-T

107163973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251900-A-G

107163973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9251900-A-T

107164108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252014-G-T

107164245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252178-C-T

http://identifiers.org/hco/13/GRCh38#107164247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9252180-A-C

107164285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252223-C-T

107164329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252264-T-G

107164516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252566-A-T

107164660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252741-C-T

107164812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252881-A-G

107164867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9252930-A-G

107165046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253052-G-A

107165046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253052-G-T

http://identifiers.org/hco/13/GRCh38#107165088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9253095-C-A

107165137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253129-A-G

http://identifiers.org/hco/13/GRCh38#107165330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9253316-C-A

107165331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253317-A-T

107165560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253531-T-G

107165631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253601-A-G

107165658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253621-G-A

107165678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253641-G-T

107165786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253748-T-C

107165982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253943-T-C

107166017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253974-T-A

107166017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9253974-T-C

107166114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254048-G-A

107166114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254048-G-T

107166655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254255-G-A

107166655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254255-G-T

http://identifiers.org/hco/13/GRCh38#107166704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9254298-A-C

107166704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254298-A-G

http://identifiers.org/hco/13/GRCh38#107166719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9254313-C-A

107166719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254313-C-G

107166719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254313-C-T

107166834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254371-G-A

107166834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254371-G-T

http://identifiers.org/hco/13/GRCh38#107166858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9254393-C-A

107166858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254393-C-T

107166882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254418-C-T

http://identifiers.org/hco/13/GRCh38#107167083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9254610-A-C

107167089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254616-T-G

107167097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254622-A-G

107167161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254688-G-T

107167468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9254953-A-G

107167601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255025-T-C

107167601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255025-T-G

http://identifiers.org/hco/13/GRCh38#107167607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255031-C-A

107167631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255054-T-C

107167728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255146-G-A

107167728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255146-G-T

107167813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255207-A-G

http://identifiers.org/hco/13/GRCh38#107167819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255213-C-A

107167819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255213-C-G

107167819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255213-C-T

http://identifiers.org/hco/13/GRCh38#107167849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255232-A-C

http://identifiers.org/hco/13/GRCh38#107167965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255370-C-A

107167965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255370-C-T

http://identifiers.org/hco/13/GRCh38#107168008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255414-C-A

107168127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255517-A-G

http://identifiers.org/hco/13/GRCh38#107168140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255530-C-A

107168153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255541-T-A

107168153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255541-T-C

107168231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255616-G-T

http://identifiers.org/hco/13/GRCh38#107168385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255703-C-A

http://identifiers.org/hco/13/GRCh38#107168390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9255712-C-A

107168407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255726-A-G

107168420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255739-G-T

107168421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9255740-T-A

http://identifiers.org/hco/13/GRCh38#107169533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9256803-C-A

107169601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9256868-G-T

107169628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9256894-T-C

107169628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9256894-T-G

107169775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257033-T-C

http://identifiers.org/hco/13/GRCh38#107169881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9257111-C-A

107169881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257111-C-G

107169881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257111-C-T

107169905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257135-G-A

107169905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257135-G-C

107169905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257135-G-T

107170019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257250-T-G

107170349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257561-G-T

107170457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257667-C-T

107170458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257668-G-A

107170458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: 3 prime UTR variant
orthologous variants: 9257668-G-T

http://identifiers.org/hco/13/GRCh38#107170882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9258120-C-A

107171235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258354-A-G

107171315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258425-G-A

107171446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258515-T-A

107171517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258593-C-T

107171530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258606-C-T

107171778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258867-T-C

http://identifiers.org/hco/13/GRCh38#107171804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9258894-C-A

107171855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9258927-G-C

107172428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9259429-T-C

http://identifiers.org/hco/13/GRCh38#107172831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9259786-A-C

107172845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9259808-T-C

107180600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9261653-C-T

107180683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9261718-T-C

107181476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262530-G-T

107181657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262744-A-T

107181753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262889-T-C

107181782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262918-T-G

http://identifiers.org/hco/13/GRCh38#107181799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9262936-A-C

107181875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262986-G-A

107181886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9262999-T-C

107182011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263079-C-T

107182190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263247-A-T

107182581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263263-T-C

107182615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263296-T-C

107182615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263296-T-G

107182648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263327-C-T

107188093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263929-C-T

107188108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9263944-C-T

107188696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9264559-G-A

107188699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9264562-T-C

107188878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9264954-T-A

107188886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9264962-G-C

107189334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9265458-A-T

107189564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9265666-A-G

http://identifiers.org/hco/13/GRCh38#107189956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9265989-C-A

107190017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266050-T-G

107190208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266219-A-G

107190303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9266314-C-G

107190308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266319-T-A

http://identifiers.org/hco/13/GRCh38#107190380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9266390-C-A

107190380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266390-C-G

107190380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266390-C-T

107190467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266465-C-T

107190611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266591-A-G

107190651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9266635-T-C

107190862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9267260-C-T

107191129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9267502-C-T

107191251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9267606-C-G

107192192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9267994-T-C

107192193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9267995-A-G

107202672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9274826-A-G

http://identifiers.org/hco/13/GRCh38#107202703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9274855-C-A

107202703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9274855-C-G

107202703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9274855-C-T

107202778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9274927-C-G

107202805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9274949-A-G

107203725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9276797-C-T

107203738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9276810-C-T

107203848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9276928-T-G

http://identifiers.org/hco/13/GRCh38#107203862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9276942-A-C

107203862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9276942-A-G

107204393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277169-C-T

107204427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277195-C-T

107204556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277303-T-C

107204556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277303-T-G

107204591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277335-T-C

107204658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277386-G-A

107204658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277386-G-C

http://identifiers.org/hco/13/GRCh38#107204681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9277406-C-A

107204681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277406-C-G

107204684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277409-C-T

107204741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277493-A-G

107204796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277545-T-C

107204996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277711-C-G

107204996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9277711-C-T

107205695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278063-C-T

107205776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278131-T-A

107205776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278131-T-G

107205790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278145-T-C

107206124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278437-T-A

107206124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278437-T-C

107206124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9278437-T-G

107208122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9281081-G-A

107208203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9281158-A-G

107210645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: synonymous variant
orthologous variants: 9282995-T-C

107210803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283152-C-G

107210803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283152-C-T

107210805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283165-G-A

107210805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283165-G-T

107210806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283166-T-A

107210806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283166-T-C

107210826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283189-G-T

http://identifiers.org/hco/13/GRCh38#107210858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9283217-C-A

107210858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283217-C-T

http://identifiers.org/hco/13/GRCh38#107210861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9283220-A-C

107210861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283220-A-G

107210886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283238-T-A

http://identifiers.org/hco/13/GRCh38#107210900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9283243-C-A

107211032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283354-G-A

107211194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9283503-G-T

107211390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283693-G-C

107211393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283696-T-C

107211418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283721-C-T

107211479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9283773-T-A

107211479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9283773-T-C

107211736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9283998-T-C

107211883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284132-C-T

107211924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284168-C-T

107211993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284223-C-T

107211994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284224-T-C

107211995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284225-G-C

107212183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284410-T-A

107212311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284532-C-G

107212472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284638-G-A

107212573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284714-G-A

107212593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284737-A-G

107212734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284871-T-C

107212734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284871-T-G

107212841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284975-G-T

107212856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9284990-C-G

107213190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285492-C-T

107213191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285493-T-G

107213224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285517-T-A

107213275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285539-G-A

107213320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285593-A-G

107213388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285680-C-T

107213425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285712-T-G

107213436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285722-C-G

107213436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285722-C-T

107213530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285799-G-A

http://identifiers.org/hco/13/GRCh38#107213663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9285931-C-A

107213690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9285962-A-G

http://identifiers.org/hco/13/GRCh38#107222045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9288145-A-C

107222078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288177-T-C

107222140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288239-G-A

107222140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288239-G-T

107222193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288285-G-A

http://identifiers.org/hco/13/GRCh38#107222257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9288375-A-C

107222285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288403-C-T

107222640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288697-A-G

107222739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9288792-G-A

107223055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289100-G-T

http://identifiers.org/hco/13/GRCh38#107223147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9289187-C-A

107223505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289424-T-A

http://identifiers.org/hco/13/GRCh38#107223647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9289545-A-C

107223734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289628-C-T

107223942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289807-C-G

107223942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289807-C-T

107224071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289877-A-G

http://identifiers.org/hco/13/GRCh38#107224108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9289921-C-A

107224132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9289945-G-A

107224175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290005-A-G

107224246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290075-T-C

107225677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290859-T-A

107225687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290870-C-T

107225689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290872-C-G

107225749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9290931-T-A

107225922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291124-C-G

107225983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291160-T-A

http://identifiers.org/hco/13/GRCh38#107226136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9291300-A-C

107226350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291515-A-G

107226350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291515-A-T

107226360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291525-G-A

107226392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291560-T-C

107226916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291630-C-G

107226916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291630-C-T

107226939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291653-T-C

107227037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291747-G-T

107227201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291898-G-A

107227202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9291899-C-T

107227393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292062-T-C

107227431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292096-C-G

107227431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292096-C-T

107227553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292218-T-C

107227814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292465-T-C

107227856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9292508-T-G

107228413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293079-C-T

107228434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293100-C-T

107228518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293169-C-T

107229275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293636-C-T

107229351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293712-T-G

http://identifiers.org/hco/13/GRCh38#107229428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9293781-C-A

107229472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293825-T-C

107229595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9293947-G-A

107229823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294153-G-T

107229845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294175-T-C

107229847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294177-C-T

107229882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294219-G-A

107229882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294219-G-T

107229975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9294302-A-G

107230747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295009-A-G

107230843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295043-T-G

107230849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295049-C-T

107230971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295125-G-A

107230971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295125-G-T

107231162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295147-G-A

http://identifiers.org/hco/13/GRCh38#107231494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9295516-C-A

107231494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295516-C-T

107231665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295652-C-T

107231666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295653-G-A

107231666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295653-G-T

107231709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295697-T-C

107231787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295766-T-A

107231787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295766-T-C

107231830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295799-A-G

107231954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9295917-T-C

107232105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296060-A-G

107232147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296102-G-T

107232166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296121-C-T

107232198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296145-G-A

107233021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296492-T-C

107233076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296539-G-C

107233151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296618-G-A

http://identifiers.org/hco/13/GRCh38#107233572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9296990-C-A

107233572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9296990-C-T

http://identifiers.org/hco/13/GRCh38#107233682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9297076-A-C

107233683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297077-T-A

107233710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297104-A-T

107233798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297176-G-A

107234143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297880-T-C

107234173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297907-A-G

107234246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297981-A-G

107234251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9297986-G-C

107234508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298220-G-A

107234508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298220-G-C

107234535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298252-C-T

107234697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298412-T-C

107234746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298432-T-C

107234885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298535-G-A

107234965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298614-C-T

107235042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298684-C-T

107235066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298705-T-G

107235135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298779-A-G

107235303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298940-C-T

107235341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9298969-C-T

107236598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9299644-G-T

107238086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9302194-G-A

107238958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303208-G-A

107239053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303299-C-G

107239116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303358-G-A

107239186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303438-A-G

107239310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303554-C-T

107239399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303653-T-C

http://identifiers.org/hco/13/GRCh38#107239448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9303694-C-A

107239484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303728-C-T

107239527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303771-C-G

107239527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303771-C-T

107239542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303785-G-A

107239574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303815-T-C

107239613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9303840-T-A

107241849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305022-G-A

107241903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305070-C-T

107241926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305098-C-T

107241940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305116-A-G

http://identifiers.org/hco/13/GRCh38#107242043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9305213-A-C

107242336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305493-G-A

107242336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305493-G-T

http://identifiers.org/hco/13/GRCh38#107242391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9305548-C-A

107242732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305907-C-T

107242825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305973-T-C

107242838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9305986-C-T

http://identifiers.org/hco/13/GRCh38#107242891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9306014-C-A

107242891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306014-C-G

107242891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306014-C-T

107242949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306065-T-C

107243085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306175-C-T

http://identifiers.org/hco/13/GRCh38#107243278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9306335-C-A

107243400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306447-C-T

107243459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306506-C-G

107243459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306506-C-T

107243484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306528-C-T

107243559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306610-C-T

107243647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306798-G-T

107243674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306927-C-T

107243732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9306988-C-T

107243909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307161-G-A

107243968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307245-T-C

107244033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307309-T-A

107244150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307424-T-G

107244198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307471-G-C

107244243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307511-G-C

107244319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307552-G-A

107244383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307603-A-G

http://identifiers.org/hco/13/GRCh38#107244422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9307645-A-C

107244443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9307664-C-T

107244834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308275-G-T

107244926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308373-T-C

107244944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308395-A-T

http://identifiers.org/hco/13/GRCh38#107245231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9308675-C-A

107245231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308675-C-G

107245393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308811-G-A

107245431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308848-C-T

107245539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9308932-A-G

107245789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9309179-T-C

http://identifiers.org/hco/13/GRCh38#107245818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9309206-C-A

107245915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9309300-G-T

107246304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9309751-C-T

107246606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9310210-T-G

107246612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9310216-T-C

107246804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9310400-T-C

107246901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9310486-T-C

107246935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9310510-G-A

107247466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311162-T-G

http://identifiers.org/hco/13/GRCh38#107247591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9311342-C-A

107247591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311342-C-T

107247801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311557-A-T

107247966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311700-C-G

107247966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311700-C-T

107247987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311717-C-T

107248068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311759-C-T

107248103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311795-T-C

107248273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9311942-A-G

107248657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9312478-C-T

107251535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314128-A-G

107251755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314330-G-T

107251932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314495-G-A

107251956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314517-C-T

107251980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314541-G-A

107252172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9314732-C-T

107252595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315020-G-T

http://identifiers.org/hco/13/GRCh38#107252633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9315054-C-A

107252633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315054-C-T

http://identifiers.org/hco/13/GRCh38#107252686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9315103-A-C

107252943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315319-T-G

107253056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315429-T-C

107253210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315558-G-T

107253467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315800-C-T

107253501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315834-C-T

107253629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9315970-A-G

107253906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316201-C-T

107253944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316236-G-A

107254116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316364-A-G

107254247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316473-A-G

107254352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316558-T-G

107254374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316578-T-C

107254537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316747-C-T

107254545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316755-C-T

http://identifiers.org/hco/13/GRCh38#107254568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9316777-C-A

107254674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316849-T-C

107254718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9316884-A-G

107254865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9317002-C-G

107255006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9317128-G-A

http://identifiers.org/hco/13/GRCh38#107255123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9317235-C-A

107255123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9317235-C-G

107255209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9317322-G-T

107263832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9323119-T-C

107263910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9323199-G-A

107263964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9323252-G-C

107266612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9324731-C-T

http://identifiers.org/hco/13/GRCh38#107266726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9324797-C-A

107266842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9324885-G-A

107267097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9325103-C-G

107267410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9325403-G-A

107267425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9325416-A-G

107267488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9325474-C-G

107268939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9326695-T-C

107269292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9326852-T-C

107269425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9326978-A-T

107269636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9327164-T-G

107269690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9327201-C-T

107270097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9327318-T-G

107270111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9327330-T-C

107270139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9327358-T-A

107273696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9332031-T-C

107274853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9335464-G-C

107274945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9335548-C-T

107275138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9335700-C-T

107276438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336182-G-T

107276636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336360-A-G

107276694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336405-T-C

107276852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336511-G-C

107277304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336959-A-T

http://identifiers.org/hco/13/GRCh38#107277330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9336989-A-C

107277330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9336989-A-G

107277532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337188-C-T

107277681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337339-A-G

http://identifiers.org/hco/13/GRCh38#107277724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9337383-C-A

107277799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337448-C-T

107277803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337452-T-C

107277837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337490-G-A

107277908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337581-C-G

107277908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9337581-C-T

107279710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9339344-C-T

107280500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9339963-T-C

http://identifiers.org/hco/13/GRCh38#107280638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9340088-C-A

107280815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9340264-T-C

107280815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9340264-T-G

107281155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9340597-C-T

107281408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9340850-G-A

107289665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9342670-A-T

107289968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9342961-G-A

107289988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9342981-G-C

107290202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9343148-G-A

107290726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9343292-T-A

107291054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9343592-A-T

http://identifiers.org/hco/13/GRCh38#107291067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9343605-C-A

http://identifiers.org/hco/13/GRCh38#107291085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9343621-C-A

107291203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9343739-C-G

107295697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9347679-T-C

107295801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9347779-C-T

107296092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9348079-C-G

107296123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9348110-T-C

107296123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9348110-T-G

http://identifiers.org/hco/13/GRCh38#107296434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9348392-A-C

107296445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9348403-G-A

107296683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349204-T-C

107296722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349240-G-A

107296738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349257-C-T

107296897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349415-A-G

107296970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349493-A-T

107297199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349681-C-T

107297242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349725-A-G

107297257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349739-C-G

107297267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349749-G-A

107297324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349809-T-C

107297363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349853-C-T

107297394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9349876-G-A

107297603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9350056-C-T

107297675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9350130-T-C

107297791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9350246-G-A

107297920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9350373-T-C

107298043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9350495-G-A

http://identifiers.org/hco/13/GRCh38#107298045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9350497-A-C

107300227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9353814-C-G

107300462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354034-G-A

107300474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354046-G-A

107300516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354087-G-A

107300876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354487-T-C

107301022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354610-G-A

107301207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354741-G-C

107301300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354818-T-C

107301305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354823-A-T

107301480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9354988-A-T

107302558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9357108-C-T

http://identifiers.org/hco/13/GRCh38#107302740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9357282-A-C

107302847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9357342-C-G

107302869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9357364-C-T

107303565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9357952-C-G

107303639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358021-T-C

107303674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358052-A-G

107304054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358338-C-T

107304192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358415-G-C

107304586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358682-G-A

107304586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358682-G-T

107304634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9358731-C-T

107304916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9359010-C-G

107305010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9359103-A-G

http://identifiers.org/hco/13/GRCh38#107308737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9361569-A-C

107308737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9361569-A-G

107308776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9361607-T-C

107309262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363173-G-C

107309262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363173-G-T

107309372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363273-T-C

http://identifiers.org/hco/13/GRCh38#107309551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9363419-A-C

107309725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363564-G-C

107309725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363564-G-T

107309859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363683-C-T

107309997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363788-C-T

http://identifiers.org/hco/13/GRCh38#107310017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9363821-C-A

107310017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9363821-C-T

107311139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364301-C-G

107311139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364301-C-T

107311267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364413-T-C

107311269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364415-C-T

107311298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364445-T-G

107311389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364523-C-G

107311488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364620-T-C

107312686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9364965-A-G

107312928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9365187-G-T

107312988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9365282-G-C

http://identifiers.org/hco/13/GRCh38#107312993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9365329-C-A

107312993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9365329-C-T

107314972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367057-T-C

107315003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367084-G-A

107315003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367084-G-T

107315109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367166-C-T

107315372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367353-T-C

107315372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367353-T-G

107316807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367880-G-A

107316839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367913-G-T

107316844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9367920-T-C

http://identifiers.org/hco/13/GRCh38#107316924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9367977-A-C

107318447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369018-C-T

107318522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369082-G-T

107318756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369312-T-A

107318765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369321-C-T

107318769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369325-G-C

107318889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369418-G-C

107318890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369419-C-T

107318954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369461-T-C

107319102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369597-C-G

107319149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369642-T-C

107319229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369715-T-C

107319370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369818-G-T

107319495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369928-T-C

107319515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9369944-T-C

107319813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370168-C-T

107319867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370225-T-A

107320275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370640-C-T

107320533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370859-A-G

107320552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370874-T-A

107320602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9370917-C-T

107320717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9371023-C-T

107320791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9371071-C-G

107320824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9371094-A-G

107320859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9371123-T-C

107321123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9371487-A-G

http://identifiers.org/hco/13/GRCh38#107321468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9371851-C-A

http://identifiers.org/hco/13/GRCh38#107321506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9371889-A-C

107321992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9372296-T-C

http://identifiers.org/hco/13/GRCh38#107322044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9372341-A-C

107322132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9372427-G-T

107322401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9372717-T-C

107322401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9372717-T-G

http://identifiers.org/hco/13/GRCh38#107322436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9372744-C-A

http://identifiers.org/hco/13/GRCh38#107322477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9372783-A-C

107322723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9373370-C-T

107323099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374365-G-A

107323202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374473-T-A

107323243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374498-A-T

107323299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374553-C-T

107323331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374583-G-T

107323424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374682-T-C

http://identifiers.org/hco/13/GRCh38#107323580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9374809-C-A

107323680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374933-C-T

107323681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9374934-G-A

107324181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9375154-T-C

107324317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9375255-C-G

107324360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9375699-C-T

107324465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9375806-C-G

107327014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376565-T-C

107327039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376591-A-G

107327111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376661-T-C

107327335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376878-G-T

107327358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376900-C-G

107327460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9376976-G-A

107327595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377106-C-G

107327681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377190-T-C

107327701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377204-T-C

107327701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377204-T-G

107327792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377295-T-C

107327813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377318-T-C

107327906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377422-C-G

107328329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377750-T-C

107328331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377752-A-G

107328342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377757-A-T

107328403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377804-A-G

107328577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377963-T-C

107328585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9377971-C-G

107328656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378037-A-G

http://identifiers.org/hco/13/GRCh38#107328822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9378180-C-A

107328822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378180-C-G

107328822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378180-C-T

107328923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378282-A-G

107328996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378342-T-C

107329023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378362-T-C

107329235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378514-A-G

107329235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378514-A-T

107329359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9378629-T-C

107330905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9380677-C-T

107331139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9380889-C-G

107331139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9380889-C-T

107331656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9381897-T-C

107331715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9381955-T-C

107333276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9383046-C-G

107333306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9383076-T-C

107333306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9383076-T-G

107334009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9383678-T-G

107334361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9384004-A-G

107334405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9384059-A-G

107334405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9384059-A-T

107335174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9385505-G-A

107335390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9385742-C-G

107335551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9385898-T-G

107335991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9386335-G-A

107336531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9386835-T-C

107336559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9386840-T-C

http://identifiers.org/hco/13/GRCh38#107336946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9387063-C-A

107336993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387107-T-C

107337008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387127-G-A

107337008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387127-G-T

107337308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387430-T-A

107337331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387451-T-C

107337471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387577-T-C

http://identifiers.org/hco/13/GRCh38#107337529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9387633-A-C

http://identifiers.org/hco/13/GRCh38#107337728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9387830-A-C

107337858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9387935-T-C

107341967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9389660-T-C

http://identifiers.org/hco/13/GRCh38#107342399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9390095-C-A

107342405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9390101-A-G

107342547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9390235-T-C

107342603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9390283-A-G

http://identifiers.org/hco/13/GRCh38#107342610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9390290-A-C

107342610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9390290-A-T

http://identifiers.org/hco/13/GRCh38#107347543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9392813-A-C

107347875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393142-C-G

107347875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393142-C-T

107347910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393177-G-A

http://identifiers.org/hco/13/GRCh38#107348058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9393322-C-A

107348058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393322-C-T

107348081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393356-T-C

107348198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393460-T-A

107348422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393677-C-T

107348461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9393725-A-G

107348665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394070-C-G

107348687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394084-T-C

107348825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394209-C-T

http://identifiers.org/hco/13/GRCh38#107349062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9394431-C-A

107349138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394511-T-C

107349290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394644-C-T

107349299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394653-G-C

107349358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394711-G-A

http://identifiers.org/hco/13/GRCh38#107350213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9394898-C-A

107350213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394898-C-G

107350213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394898-C-T

107350264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9394948-G-A

107360121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9395975-A-G

107360252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9396107-G-A

http://identifiers.org/hco/13/GRCh38#107360288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9396143-C-A

107364532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397463-T-G

107364571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397497-C-T

107364659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397587-C-G

107364698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397625-C-T

107364749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397667-G-T

107365141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397814-C-T

107365160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397833-A-G

107365165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9397838-G-A

107373706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9398989-T-C

107373911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9399157-T-C

107374089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9399337-A-G

http://identifiers.org/hco/13/GRCh38#107374494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9399688-C-A

107374513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9399712-A-G

107375069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400059-T-C

107375131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400116-T-G

107375186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400170-G-A

107375439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400395-A-G

107375448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400404-A-G

107375542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400497-C-G

107375542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400497-C-T

107375577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400516-T-A

107375578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400517-T-A

107375927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400814-C-T

107376104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9400959-C-T

107378317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9408688-C-T

107378328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9408699-T-C

107378367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9408738-T-C

http://identifiers.org/hco/13/GRCh38#107378422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9408766-A-C

107378422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9408766-A-G

107378508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9408824-G-C

107379029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409282-C-T

107379208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409433-T-G

107379400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409619-T-G

http://identifiers.org/hco/13/GRCh38#107379477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9409682-C-A

107379489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409694-G-C

107379491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409696-A-T

107379494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9409699-T-C

107379940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410204-C-T

107380149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410390-G-C

107380149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410390-G-T

107380190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410429-T-G

107380280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410561-G-A

107380343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9410624-A-G

107382457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9412629-C-T

107382507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9412675-C-T

107382557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9412722-T-C

107382625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9412770-T-C

107382667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9412816-A-G

107382886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413040-A-T

107383026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413178-T-C

107383172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413323-G-A

http://identifiers.org/hco/13/GRCh38#107383191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9413342-A-C

107383302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413439-T-C

107383584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413725-A-T

107383620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9413770-G-T

107383895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9414031-C-T

http://identifiers.org/hco/13/GRCh38#107384599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9414319-A-C

107384599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9414319-A-G

107384964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9414683-T-C

http://identifiers.org/hco/13/GRCh38#107385699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9415249-C-A

107385754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9415855-T-C

107386138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416211-T-C

107386275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416326-T-A

107386275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416326-T-C

107386291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416342-C-T

107386308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416355-C-G

107386308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416355-C-T

107386309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416356-T-C

107386393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416435-G-A

107386552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416551-T-G

107386835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9416815-T-C

107387233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9417128-C-T

107387292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9417187-T-C

http://identifiers.org/hco/13/GRCh38#107387455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9417364-C-A

107387576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9417502-C-T

107387742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9417668-C-T

107387847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9417773-T-C

107393914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421227-G-A

107393914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421227-G-T

107393978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421288-C-T

107394004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421312-T-C

107394038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421335-T-A

107394098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421398-T-C

107394346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421814-G-A

107394347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421815-G-T

107394442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421931-G-A

107394490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9421979-A-G

107394522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422011-G-A

107394523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422012-T-A

107394650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422137-C-T

107394652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422139-T-C

107394760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422242-T-C

107394867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422340-G-A

http://identifiers.org/hco/13/GRCh38#107394980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9422442-A-C

107395063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422522-G-T

107395158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422616-T-C

107395235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422691-T-A

http://identifiers.org/hco/13/GRCh38#107395242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9422698-A-C

107395242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422698-A-G

107395288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422709-G-C

107395303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422729-T-C

107396818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9422907-C-T

107396947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423027-C-T

107396949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423029-T-C

107397015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423090-T-C

107397165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423243-C-T

107397247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423325-T-C

http://identifiers.org/hco/13/GRCh38#107397249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9423327-C-A

107397306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9423380-T-C

107397685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9424923-T-G

107398149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425364-C-T

107398307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425513-A-G

http://identifiers.org/hco/13/GRCh38#107398317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9425525-A-C

107398317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425525-A-T

http://identifiers.org/hco/13/GRCh38#107398376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9425583-A-C

107398507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425693-G-T

107398733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425890-A-G

107398794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9425937-G-A

107398945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426080-C-T

107398969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426103-C-T

http://identifiers.org/hco/13/GRCh38#107399198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9426265-A-C

107399240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426311-G-A

107399390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426446-G-A

http://identifiers.org/hco/13/GRCh38#107399391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9426447-C-A

107399391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426447-C-T

107399603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426743-C-G

107399606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9426747-C-T

107399890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9427943-A-G

107399899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9427952-A-G

107399909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9427962-T-C

107400000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9428066-T-G

http://identifiers.org/hco/13/GRCh38#107400058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9428123-A-C

107400066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9428131-C-G

107400076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9428141-T-C

107400076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9428141-T-G

107403618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9431838-T-C

107403686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9431905-C-T

107403766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9431984-G-A

107403891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9432143-T-C

107403975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9432334-A-T

http://identifiers.org/hco/13/GRCh38#107404073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9432442-A-C

107404098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9432467-G-T

107404159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9432514-T-C

107404234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9432593-G-A

http://identifiers.org/hco/13/GRCh38#107404644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9432991-A-C

107410846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9434659-C-T

107410891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9434720-G-A

http://identifiers.org/hco/13/GRCh38#107411077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9434878-C-A

107412266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9436702-A-T

107412267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9436703-C-T

107412611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9437006-G-A

107412641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9437042-T-A

107412895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9437855-G-T

107412913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9437871-T-G

107413288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9438359-C-T

107413308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9438379-G-A

http://identifiers.org/hco/13/GRCh38#107415408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9444789-C-A

107415410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9444791-G-T

107415813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9445204-G-C

107415849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9445227-A-G

107415874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9445252-C-G

107415906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9445287-T-A

107415929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9445317-C-T

http://identifiers.org/hco/13/GRCh38#107419906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9446712-C-A

107419906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9446712-C-T

107419933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9446739-T-C

http://identifiers.org/hco/13/GRCh38#107420220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9447031-A-C

107420232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447040-T-C

107420326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447159-T-G

107420447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447272-T-C

http://identifiers.org/hco/13/GRCh38#107422786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9447657-A-C

107422786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447657-A-G

107422880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447730-G-A

107423122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447938-T-C

107423187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9447999-G-C

107423205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9448017-A-G

107423206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9448018-T-C

107423314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9448125-A-G

107423658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9448419-T-G

107425021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9452120-T-A

107426669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9453088-A-T

107426774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9453193-C-T

107427077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9453531-G-A

107427218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9453669-T-C

107427453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9453897-T-G

107427549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9454006-G-A

107427637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9454087-C-G

107427637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9454087-C-T

107427823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9454260-G-A

http://identifiers.org/hco/13/GRCh38#107429371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9455105-A-C

107429371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9455105-A-G

107429425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9455156-C-T

107429615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9455336-T-C

107444062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9461341-T-C

107444295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9461560-T-G

107444386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9461632-A-G

107446653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9462309-T-C

107447582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463562-C-T

107447646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463628-C-G

107447663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463645-T-C

107447667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463649-A-T

107447731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463710-G-A

107447788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9463764-A-G

107448129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464083-C-T

107448253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464198-C-T

107448261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464210-T-G

http://identifiers.org/hco/13/GRCh38#107448368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9464886-C-A

107448368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464886-C-T

107448394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464908-G-A

107448443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9464960-C-T

107448496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465008-G-A

107448574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465067-T-G

107448575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465068-G-A

107448618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465105-T-C

107448835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465346-G-T

107448843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465354-C-T

107448882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465393-T-C

107448884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465395-T-C

107449266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465454-A-G

107449416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465602-G-T

http://identifiers.org/hco/13/GRCh38#107449464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9465650-C-A

107449464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465650-C-T

http://identifiers.org/hco/13/GRCh38#107449511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9465699-A-C

107449511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465699-A-T

107449729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465896-C-T

107449763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9465930-C-T

107449855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466005-G-C

107449916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466062-A-G

107449969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466112-T-A

107449969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466112-T-G

107450058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466190-A-G

107450100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466229-T-C

107450414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466689-G-T

107450486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466759-A-G

107450692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9466923-C-T

107451015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9467246-C-G

107451340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9467520-T-C

107456323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9468328-C-T

107456537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9468528-G-A

107456577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9468562-C-T

107456607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9468593-T-C

107457101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469021-G-T

107457181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469088-G-C

107457449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469425-G-A

107457627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469600-A-G

107457815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469790-G-A

107457879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9469856-T-C

107458174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9470137-T-A

107475700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9476949-T-C

107475717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9476972-G-A

107475727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9476982-G-A

107475727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9476982-G-T

107475747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477007-G-C

107475774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477034-A-G

107476363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477391-T-G

107476442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477471-C-T

107476458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477478-T-C

107476520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9477540-T-C

107477055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478037-A-T

107477095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478063-T-C

107477095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478063-T-G

107477333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478280-T-C

107477514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478438-T-C

http://identifiers.org/hco/13/GRCh38#107477544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9478452-A-C

107477688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478591-C-T

107477782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478692-G-A

107477896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9478866-T-C

http://identifiers.org/hco/13/GRCh38#107477907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9478877-A-C

107478080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9479037-A-G

http://identifiers.org/hco/13/GRCh38#107478255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9479186-C-A

107478324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9479247-C-G

107478324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9479247-C-T

107478405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9479286-C-G

107478714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9479765-C-T

107478899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480007-G-T

107479060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480166-A-G

107479239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480336-T-C

107479252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480350-G-A

107479569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480596-G-T

107479623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9480646-G-T

107479902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9481014-T-A

107480200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9481270-C-T

107480253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9481330-G-A

107480317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9481384-G-A

107480976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9482093-G-A

107481094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9482214-C-G

107481098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9482218-C-G

http://identifiers.org/hco/13/GRCh38#107481833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9482770-A-C

http://identifiers.org/hco/13/GRCh38#107481834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9482771-C-A

107481857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9482793-C-T

107482072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9482991-T-A

107482269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483169-C-T

107482502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483349-G-A

107482505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483352-T-C

107482528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483379-A-T

107482604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483502-T-C

107482660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483562-G-A

107482660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483562-G-T

107482679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483579-T-C

107482837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483696-A-G

107482837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9483696-A-T

107483866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484282-A-G

107483879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484295-G-A

107483930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484361-G-T

107483968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484407-A-G

http://identifiers.org/hco/13/GRCh38#107483976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9484415-C-A

107484045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484489-G-A

http://identifiers.org/hco/13/GRCh38#107484097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9484539-C-A

107484176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484617-T-C

107484379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9484812-G-C

107484607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9485625-T-G

107484624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9485642-G-C

http://identifiers.org/hco/13/GRCh38#107484662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9485682-C-A

107484982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486000-C-T

107485018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486035-C-T

107485023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486040-A-G

107485038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486055-C-T

107485245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486234-G-A

107485287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486262-G-A

107485396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486360-C-T

107485398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9486362-A-G

107490746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488063-C-T

107490828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488142-G-A

http://identifiers.org/hco/13/GRCh38#107490970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9488295-C-A

107490970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488295-C-T

107491002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488328-A-G

107491442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488921-C-G

107491442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9488921-C-T

http://identifiers.org/hco/13/GRCh38#107491628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9489151-A-C

http://identifiers.org/hco/13/GRCh38#107491639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9489162-A-C

107491867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9489386-G-T

107491993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9489528-C-G

107492610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9489808-C-T

107492726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9489910-G-T

107492811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9489991-G-A

http://identifiers.org/hco/13/GRCh38#107492842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9490020-C-A

107492842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490020-C-T

http://identifiers.org/hco/13/GRCh38#107493074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9490252-A-C

107493125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490307-T-C

107493377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490523-G-A

107493530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490689-T-C

107493692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490821-C-T

107493715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9490845-A-T

107494312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9491298-A-T

107494345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9491331-C-T

107494351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9491337-T-C

http://identifiers.org/hco/13/GRCh38#107494622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9492551-C-A

107494622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9492551-C-G

107494649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9492575-G-A

http://identifiers.org/hco/13/GRCh38#107494740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9492656-C-A

http://identifiers.org/hco/13/GRCh38#107494753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9492691-C-A

107494816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9492749-T-C

107495053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9492946-C-T

107495287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493135-C-G

107495322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493175-T-C

107495340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493193-G-A

107495340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493193-G-C

107495352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493207-T-C

107495631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493571-T-A

107495676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493618-A-T

http://identifiers.org/hco/13/GRCh38#107495731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9493668-C-A

107495733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493670-T-C

107495738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493678-G-T

107495779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493718-G-A

107495837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493786-G-A

http://identifiers.org/hco/13/GRCh38#107495844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9493791-A-C

107495845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493792-G-C

107495874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493818-A-G

107495894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9493838-T-A

107496194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9494112-G-C

107497113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9494648-T-G

107497485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495001-T-C

107497490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495006-G-A

107497576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495076-T-A

107497871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495550-C-T

107498058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495738-T-C

http://identifiers.org/hco/13/GRCh38#107498076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9495751-C-A

107498160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495836-A-G

107498306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9495973-G-A

107498399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496060-G-A

107498472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496133-T-A

107498493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496154-A-G

107498524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496185-A-T

107498600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496258-G-A

107498600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496258-G-C

107498679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496335-A-G

107498760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496415-T-G

107498830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496464-G-C

107498987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496636-A-G

107499009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9496658-T-C

107501825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9499147-T-G

107502015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9499317-G-T

107502645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500125-T-C

http://identifiers.org/hco/13/GRCh38#107502646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9500126-A-C

107502744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500247-T-C

107502794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500310-T-C

107502852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500373-T-C

107502948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500475-A-G

http://identifiers.org/hco/13/GRCh38#107503016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9500532-A-C

107503090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500606-T-A

107503161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500661-T-G

107503198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500698-T-C

107503254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500748-C-G

107503278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9500771-T-C

107505845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9501570-A-G

107505851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9501576-A-T

107505858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9501583-G-A

107506072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9501998-A-G

107506403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9502548-G-A

107506621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9502784-C-T

107506680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9502829-T-C

107506836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9502986-A-G

107506877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503028-T-A

107506897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503055-C-G

107506899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503057-T-C

107506958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503109-A-G

107507001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503141-T-C

107507050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503190-T-C

107507050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503190-T-G

107507417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503403-T-C

107507419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503405-T-C

107507496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503504-T-C

107507543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503566-A-T

107507563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503576-T-C

107507564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503577-G-T

107507573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503587-G-A

107507573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503587-G-T

http://identifiers.org/hco/13/GRCh38#107507590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9503604-C-A

107507590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503604-C-T

http://identifiers.org/hco/13/GRCh38#107507634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9503628-A-C

http://identifiers.org/hco/13/GRCh38#107507637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9503631-C-A

107507838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503840-G-A

107507926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9503927-A-G

107508486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504705-G-C

107508486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504705-G-T

107508518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504737-G-A

107508560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504778-C-T

107508591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504823-T-C

107508666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9504896-T-C

107508936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505483-G-C

107509080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505619-G-A

107509087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505626-T-C

107509184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505727-G-T

107509287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505824-A-G

107509291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505828-G-A

107509381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505917-G-A

107509424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9505998-T-C

http://identifiers.org/hco/13/GRCh38#107509455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9506028-A-C

107510588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9506780-A-G

107510612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9506806-T-C

http://identifiers.org/hco/13/GRCh38#107510753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9506953-C-A

107510753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9506953-C-G

107510820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507022-C-G

107510839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507039-G-T

107510851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507047-G-C

107511051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507218-C-T

107511055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507222-T-C

107511103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9507268-C-T

http://identifiers.org/hco/13/GRCh38#107511513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9507732-C-A

107513512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509127-G-T

107513538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509153-A-G

107513618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509242-C-T

107513731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509350-G-A

107513731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509350-G-C

107514011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509582-G-A

107514320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9509825-G-A

http://identifiers.org/hco/13/GRCh38#107514984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9510207-C-A

107515009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510225-G-A

107515119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510354-G-A

107515159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510385-G-A

107515296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510469-G-A

107515446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510615-T-C

107515649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510815-C-T

http://identifiers.org/hco/13/GRCh38#107515793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9510956-C-A

107515793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9510956-C-T

107516455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9512017-G-C

107516498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9512056-T-C

107516524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9512084-C-G

107516592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9512145-G-A

107518083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514150-G-A

http://identifiers.org/hco/13/GRCh38#107518130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9514209-A-C

107518441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514526-G-T

107518627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514710-T-C

107518634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514717-C-T

107518701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514813-G-A

107518748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514882-T-A

107518845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9514988-G-A

http://identifiers.org/hco/13/GRCh38#107518864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9515008-C-A

http://identifiers.org/hco/13/GRCh38#107518877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9515021-A-C

107518939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515077-T-C

107519160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515254-G-A

107519197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515289-C-T

107519459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515502-T-C

107519459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515502-T-G

107519542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515562-G-A

http://identifiers.org/hco/13/GRCh38#107519689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9515673-A-C

107519879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9515842-T-C

http://identifiers.org/hco/13/GRCh38#107519953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9515920-C-A

http://identifiers.org/hco/13/GRCh38#107519961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9515929-A-C

107520351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516210-A-G

107520383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516241-G-T

107520508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516375-G-A

107520536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516406-G-A

107520604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516479-T-G

107520857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516818-G-A

107520862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516823-T-C

107520883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9516848-C-G

http://identifiers.org/hco/13/GRCh38#107521059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9517228-A-C

107521167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9517317-A-G

107521263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9517394-C-G

107521273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9517405-C-T

107521419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9517549-C-T

http://identifiers.org/hco/13/GRCh38#107521934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9519570-C-A

107521942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9519578-T-C

107521976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9519612-C-T

107522219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9519850-G-A

107523104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9520273-G-A

107523122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9520293-C-T

107523177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9520343-G-A

107524001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9520879-C-T

107524507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9521297-A-G

107524775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9521577-C-T

107525058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9521843-T-C

107525120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9521904-C-G

107525120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9521904-C-T

107526356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524218-C-T

107526446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524306-G-A

107526684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524510-C-G

107526684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524510-C-T

107526881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524699-G-A

107526976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524795-T-C

107526993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524812-T-C

107527037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524854-T-C

107527161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9524979-T-C

107527312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9525126-G-T

107527314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9525128-T-C

107527952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9525262-T-C

107528056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9525383-C-T

107529134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526242-C-T

107529265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526352-T-C

107529335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526407-G-A

107529335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526407-G-T

http://identifiers.org/hco/13/GRCh38#107529376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9526450-A-C

107529554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526608-G-A

107529690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526729-T-C

http://identifiers.org/hco/13/GRCh38#107529717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9526756-C-A

107529835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526855-C-T

107529839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526859-C-G

107529859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526879-G-C

107529949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9526961-G-A

107530026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527034-T-C

107530108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527124-C-G

107530108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527124-C-T

107530218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527195-C-T

107530419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527371-G-A

107530500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527551-A-G

107530594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527644-G-C

107530605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527654-C-T

107530652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527701-G-T

107530768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527803-C-T

107530913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527962-G-A

107530920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9527969-A-T

107531544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528313-T-C

107531544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528313-T-G

107531829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528513-T-C

107531870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528557-A-G

107531875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528562-T-C

107531959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528644-C-T

107532177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9528866-A-G

107532505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9529065-C-T

107532643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9529192-T-C

107532740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9529291-A-G

107532867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9529429-C-T

107532880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9529441-A-G

107538646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9530809-G-A

107538816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9530957-A-G

107541050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532529-C-G

107541050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532529-C-T

http://identifiers.org/hco/13/GRCh38#107541073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9532552-C-A

http://identifiers.org/hco/13/GRCh38#107541076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9532555-A-C

107541076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532555-A-T

107541117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532596-A-G

107541142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532621-T-G

107541238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9532719-G-C

107541592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9533014-T-C

107541662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9533084-G-A

107541696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9533576-G-T

http://identifiers.org/hco/13/GRCh38#107541721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9533601-C-A

http://identifiers.org/hco/13/GRCh38#107541848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9533704-C-A

107542487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9534489-T-C

107542555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9534571-T-C

107542576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9534607-C-T

107542584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9534615-A-G

http://identifiers.org/hco/13/GRCh38#107542898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9534898-A-C

107542916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9534915-T-C

107543026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9535011-T-A

107543057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9535069-A-T

107543118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9535142-C-T

http://identifiers.org/hco/13/GRCh38#107543345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9535459-C-A

107543842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9535637-C-T

107544340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536092-T-C

http://identifiers.org/hco/13/GRCh38#107544568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9536316-A-C

107544615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536365-C-T

107544711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536459-G-A

107544907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536637-G-A

107545051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536769-C-T

107545075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536792-A-T

107545080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536797-G-C

107545294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9536986-G-A

107545333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537034-T-C

107545361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537063-C-T

107545576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537223-G-T

107548656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537543-G-C

107548727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537609-C-T

107548729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537611-T-C

107548810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537695-A-T

107548956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537829-T-C

107548983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537856-C-G

107548983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9537856-C-T

107550721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538359-T-C

107550788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538423-T-C

107550957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538561-T-G

107550990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538594-T-C

107551043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538647-C-G

107551176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9538770-C-T

107551574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9539720-G-C

http://identifiers.org/hco/13/GRCh38#107551638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#9539787-C-A

107551740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9539880-T-A

107551809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9539945-G-A

107551828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9539973-T-C

107551870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540020-T-A

107551870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540020-T-C

107552029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540255-T-C

107552032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540258-A-G

107552036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540262-A-T

107552144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540372-G-A

107552169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540398-A-G

107552209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540443-G-C

107552393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540629-G-A

107552393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540629-G-C

107552435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540671-G-A

107552435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540671-G-C

107552435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540671-G-T

107552465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540701-T-C

107552550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540774-T-A

107552599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540818-C-T

107552600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9540819-T-C

107553230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541623-T-C

107553285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541674-T-A

107553340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541780-G-A

107553342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541782-A-G

107553362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541799-T-C

107553562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9541979-A-T

107553697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9542123-C-T

107553718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9542145-A-G

107553972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9542331-G-C

107554081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9542409-G-T

107554612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9543811-T-A

107554612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9543811-T-C

107554782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9543949-A-G

107554897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9544070-A-G

107554940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron_variant, undefined
orthologous variants: 9544177-T-C

107556887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9545381-G-A

107557965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9548440-G-A

107557965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9548440-G-C

107558041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9548516-A-G

107558089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9548561-A-G

http://identifiers.org/hco/13/GRCh38#107561018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9550135-C-A

107561018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9550135-C-T

107561096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9550206-G-A

107563400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9550692-T-A

107563504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9550788-C-T

107563650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33877
most severe consequence: intron variant
orthologous variants: 9550905-C-G