107787898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9747619-C-T

http://identifiers.org/hco/13/GRCh38#107788216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749153-A-C

http://identifiers.org/hco/13/GRCh38#107788479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749386-C-A

107788479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749386-C-G

107788493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749400-T-C

http://identifiers.org/hco/13/GRCh38#107788494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749401-C-A

107788507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749414-G-A

107788507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749414-G-T

http://identifiers.org/hco/13/GRCh38#107788625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749544-A-C

107788625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749544-A-G

http://identifiers.org/hco/13/GRCh38#107788646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749565-C-A

107788691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749608-A-G

107788771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749651-T-C

http://identifiers.org/hco/13/GRCh38#107788986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9749837-C-A

107788986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749837-C-T

107789047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749895-A-G

107789077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749913-G-T

107789084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9749920-G-A

107789116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9749951-T-C

107789153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9749959-T-A

107789171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9749977-T-A

107789171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9749977-T-C

107790334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750506-T-C

107790473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750638-G-A

107790732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750875-C-T

107790744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750887-C-T

107790775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750916-T-A

107790775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9750916-T-C

107790921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751127-G-A

107790921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751127-G-T

107790947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751153-G-A

107790950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751156-T-C

http://identifiers.org/hco/13/GRCh38#107791000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9751197-A-C

http://identifiers.org/hco/13/GRCh38#107791074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9751262-A-C

107791140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751335-T-C

107791258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9751447-G-A

107791376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9752231-A-T

107791429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9752284-C-T

http://identifiers.org/hco/13/GRCh38#107792317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9753077-A-C

http://identifiers.org/hco/13/GRCh38#107793056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9753387-A-C

107793158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753496-T-C

107793181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753518-C-G

107793193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753530-A-G

107793199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753536-T-A

107793287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753614-C-T

107793470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9753705-T-C

http://identifiers.org/hco/13/GRCh38#107793939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9754088-A-C

107794169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754235-T-C

http://identifiers.org/hco/13/GRCh38#107794180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9754246-C-A

107794198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754257-G-A

107794201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754260-C-G

107794315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754360-T-G

107794465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754507-T-C

107794487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754538-G-T

107794494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754546-T-C

107794525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754579-T-C

http://identifiers.org/hco/13/GRCh38#107794554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9754594-C-A

107794681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754692-T-C

107794682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754693-A-G

http://identifiers.org/hco/13/GRCh38#107794714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9754724-C-A

107794714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754724-C-G

http://identifiers.org/hco/13/GRCh38#107794816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9754824-C-A

107794816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754824-C-T

107794942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754948-T-C

107794969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9754975-G-A

http://identifiers.org/hco/13/GRCh38#107796006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9755368-A-C

107796215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755542-T-C

107796225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755552-G-C

107796264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755591-T-C

107796363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755663-T-C

107796494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755788-G-T

107796625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9755949-C-T

http://identifiers.org/hco/13/GRCh38#107796856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9756174-A-C

http://identifiers.org/hco/13/GRCh38#107796878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9756196-A-C

107798160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9756619-G-A

107798207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9756659-T-C

107798449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9756883-T-C

107798482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9756916-T-C

107798840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757213-C-G

107798840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757213-C-T

107798978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757346-A-G

107799185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757525-C-G

107799324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757660-A-G

107799569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757919-A-T

107799609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9757957-G-A

107799780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9758114-G-A

107799889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9758210-T-C

107799970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9758279-A-G

107800925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759374-A-G

http://identifiers.org/hco/13/GRCh38#107801239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9759696-A-C

107801264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759729-T-C

107801466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759924-G-A

107801466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759924-G-T

107801616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760073-T-G

http://identifiers.org/hco/13/GRCh38#107801657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9760115-C-A

107801657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760115-C-T

107801662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760120-T-C

107801893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760337-A-G

107802024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760460-G-A

107802024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760460-G-T

107802073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760514-A-G

107802145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760592-A-T

107802276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760741-C-G

107802491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761296-A-G

107802501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761306-T-A

107802506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761311-G-A

107803158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762345-T-C

107803234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762416-G-A

107803325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762504-C-T

107803335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762514-T-G

107803389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762563-C-T

107803581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762766-T-A

107803753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762929-G-A

107806835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763994-T-C

107806889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764050-T-A

http://identifiers.org/hco/13/GRCh38#107807061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9764213-C-A

107807061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764213-C-T

107807068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764224-A-G

107807137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764321-A-T

107807335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764502-T-C

107807493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764628-T-C

107807498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764633-G-T

107807574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764708-G-A

107807860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764992-T-C

107812812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9767174-T-C

107813046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9767306-C-T

107816785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769277-T-C

107816936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769414-T-C

107816936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769414-T-G

http://identifiers.org/hco/13/GRCh38#107816961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9769446-A-C

107817057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769546-A-G

http://identifiers.org/hco/13/GRCh38#107817165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9769648-A-C

107817208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769688-T-C

107817210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769690-T-C

107817223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769703-G-A

107817223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769703-G-C

107817223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769703-G-T

http://identifiers.org/hco/13/GRCh38#107817295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9769776-C-A

107817295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769776-C-T

107819987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771401-G-A

107820183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771639-C-T

107820244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771700-G-A

107820305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771761-T-G

107820595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772052-T-C

107820682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772140-A-G

107820873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772726-C-T

107821062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772908-A-G

107821155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773003-T-C

107821335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773185-T-C

107821365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773197-A-G

107821629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773345-A-G

107821810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773513-T-C

107823660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775220-C-G

107823703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775256-C-G

107823751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775301-A-G

107823769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775319-C-T

107823857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775412-A-G

107824008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775548-G-T

107824256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775750-A-G

107824451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775898-G-A

107824509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775936-T-C

107824591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775986-T-C

107824661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776056-G-T

http://identifiers.org/hco/13/GRCh38#107824678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9776073-C-A

107825243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776593-G-C

107825248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776598-A-G

107825415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776749-C-T

107826298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9777997-T-C

107826481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778215-T-C

107826498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778224-T-C

107826605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778295-G-A

107826726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778417-G-A

107826734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778425-G-A

107826835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778523-T-C

107826855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778547-G-A

107827262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9778965-T-C

107827315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779034-T-C

107827324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779043-T-G

107827420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779136-C-T

107827421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779137-G-A

107828053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779327-G-A

107828148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779428-G-A

107828243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779513-A-G

107828347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779614-C-T

107828350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779617-A-G

107828610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9779764-C-T

107828879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780022-C-T

107828916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780057-T-A

107829145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780349-G-C

107829438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780586-A-G

107829736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780830-G-A

107829759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780839-G-C

107829864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780946-G-C

107829864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9780946-G-T

107830027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9781092-A-G

107833801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9784649-C-T

107834440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9784867-A-G

107834625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785050-G-A

107835023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785435-A-G

107835023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785435-A-T

107835207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785621-A-G

107835317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785732-T-C

http://identifiers.org/hco/13/GRCh38#107835320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9785735-C-A

107835334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785749-G-C

http://identifiers.org/hco/13/GRCh38#107835373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#9785787-C-A

107835396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9785810-A-T