104491225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945993-G-A

104491509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945712-G-A

104491509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945712-G-T

104491528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945693-T-C

104491744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945477-T-G

104491863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945358-G-A

104491863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945358-G-C

104491863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945358-G-T

104491880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945341-G-A

104491880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945341-G-T

104491887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945334-G-A

104491887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945334-G-C

104491887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945334-G-T

104491891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945330-G-A

104491891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945330-G-T

104491905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945316-G-A

104491905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945316-G-T

104491908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945313-G-A

104491908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945313-G-T

104492092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945129-A-T

104492144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945074-A-G

http://identifiers.org/hco/4/GRCh38#104492205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133945010-C-A

104492205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133945010-C-T

http://identifiers.org/hco/4/GRCh38#104492239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133944982-C-A

104492239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944982-C-T

http://identifiers.org/hco/4/GRCh38#104492278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133944932-C-A

104492278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944932-C-G

104492465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133944743-G-C

104492465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133944743-G-T

104492818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944394-T-C

104493071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944087-C-T

104493102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944056-T-G

http://identifiers.org/hco/4/GRCh38#104493224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133943931-A-C

104493234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943921-C-T

104493449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943713-T-G

104493540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943621-G-A

104493613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943549-C-T

104494361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942798-G-A

104494664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-A

104494664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-C

104494664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-T

104494665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-A

104494665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-C

104494665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-T

104494796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133942349-G-T

104494929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942210-T-C

104494938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942198-T-C

104494968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942168-T-C

http://identifiers.org/hco/4/GRCh38#104494969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133942167-C-A

104495023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942114-G-A

104495023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942114-G-C

http://identifiers.org/hco/4/GRCh38#104495065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133942074-C-A

104495138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942021-G-A

104495609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941543-G-A

104495758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941364-C-T

104495976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941163-G-T

104496511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940530-T-C

104496641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940420-A-G

104497036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940121-G-T

104497077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940078-A-T

104497591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133939594-G-A

104497832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133939384-A-G

104498129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133939280-T-G

104498324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133939103-C-T

http://identifiers.org/hco/4/GRCh38#104499329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133938657-C-A

104499330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938656-T-C

104499412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938586-T-C

104499582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938442-T-C

104499659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938346-C-G

104501367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133935489-T-G

104501368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133935488-T-G

http://identifiers.org/hco/4/GRCh38#104501419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133935437-C-A

104501476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133935378-G-C

104501696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133935239-A-G

104502163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133934785-T-C

104502352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133934641-A-G

104502543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133934466-G-A

104502669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133934342-T-C

104502807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133934207-T-C

http://identifiers.org/hco/4/GRCh38#104502854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133934164-A-C

104503074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133933933-G-A

104503084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133933923-C-T

104503218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133933810-T-C

104503377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133932651-T-G

104503722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133932334-T-G

104503980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133932083-C-T

104504128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133931953-A-T

104504232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133931853-T-C

104504364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133930270-A-G

104504514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133930106-A-T

104504878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133929742-T-C

104505812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133928855-G-T

104505888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133928811-T-C

104506098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133928588-T-A

104506514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133928236-C-T

104506660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133928102-A-G

104506781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927987-A-G

104506981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927785-T-C

104507019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927748-G-A

http://identifiers.org/hco/4/GRCh38#104507049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133927719-C-A

104507049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927719-C-T

104507367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927448-C-T

104507415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927400-G-T

104507517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927316-T-C

104507816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927039-C-T

104507838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133927017-T-C

104508088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926745-T-C

http://identifiers.org/hco/4/GRCh38#104508146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133926686-C-A

104508146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926686-C-G

104508187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926650-G-A

104508310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926529-T-G

104508322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926517-G-A

104508469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926384-A-G

104508503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926352-C-T

104508634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926217-A-G

104508768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133926080-G-A

http://identifiers.org/hco/4/GRCh38#104511070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133925016-C-A

104511154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924930-T-G

104511212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924872-G-A

104511212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924872-G-T

104511220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924864-G-A

104511341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924763-T-C

http://identifiers.org/hco/4/GRCh38#104511402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133924717-A-C

104511568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924560-G-A

104511701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924436-G-A

http://identifiers.org/hco/4/GRCh38#104511837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133924310-C-A

104511984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924159-C-T

104512204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923940-G-A

http://identifiers.org/hco/4/GRCh38#104512268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133923872-A-C

104512268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923872-A-T

104512279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923861-T-C

104512563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923664-G-A

104513031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923215-G-T

104513158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923101-T-C

104513308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133922936-T-G

104513545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133922704-G-A

104513702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133922536-C-T

104516916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921287-A-G

104516917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921286-A-G

104516918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921285-T-A

104516919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921284-A-G

104517016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921194-G-T

104517074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921144-G-A

http://identifiers.org/hco/4/GRCh38#104517103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133921115-C-A

104520079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133917863-C-T

104520195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133917741-C-T

http://identifiers.org/hco/4/GRCh38#104520227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133917709-C-A

104520227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133917709-C-G

104520308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133917617-T-A

104520336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133917598-C-G

104520879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133917112-G-C

104520987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916998-T-C

104521165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916718-C-T

104521449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916406-A-G

104521468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916391-A-G

104521641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916220-A-G

104521720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133916149-T-C

http://identifiers.org/hco/4/GRCh38#104522953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133915795-C-A

104523023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915726-T-C

104523347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915289-T-C

104523351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915285-G-C

http://identifiers.org/hco/4/GRCh38#104523395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133915264-A-C

104523399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915260-G-C

104523403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915256-G-A

104523403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915256-G-T

http://identifiers.org/hco/4/GRCh38#104523513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133915149-A-C

104523513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915149-A-G

104523625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915030-A-G

104523646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133915005-A-G

104523831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914822-T-C

104523831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914822-T-G

104523867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914786-A-G

104523869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914785-C-T

104524022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914638-T-C

104524071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914602-A-G

104524388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914310-T-C

http://identifiers.org/hco/4/GRCh38#104524435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133914284-C-A

104524519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914213-G-A

104524571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914175-A-G

104524594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914152-C-G

104524603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133914143-T-G

http://identifiers.org/hco/4/GRCh38#104529890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133913387-A-C

104530040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133913256-T-C

104530068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133913226-G-T

104530104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133913186-T-G

104530201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133913081-G-A

http://identifiers.org/hco/4/GRCh38#104530241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133913041-C-A

104530254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133913028-G-A

104530324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912963-C-T

104530586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912708-C-T

104530807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912489-G-A

104530916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912396-A-T

104531088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912235-T-A

104531088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912235-T-G

104531146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912179-T-C

http://identifiers.org/hco/4/GRCh38#104531414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133911939-A-C

104531444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911910-T-C

104531611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911701-C-T

104531626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911686-A-G

104531626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911686-A-T

http://identifiers.org/hco/4/GRCh38#104531654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133911653-A-C

104531662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911582-T-C

104531717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911511-G-T

104532139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911163-A-G

104532193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911103-T-C

104532213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911082-T-C

104532621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908879-G-A

104533134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908417-T-G

104533239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908315-T-A

104533728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907846-G-T

104533737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907839-T-C

104533940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907390-G-A

104533999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907321-G-A

104534177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907149-C-T

104534303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907033-T-C

104534466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133906892-G-A

104537673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903740-T-C

104537686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903727-C-G

104538044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903499-T-C

http://identifiers.org/hco/4/GRCh38#104538839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133902510-A-C

104538979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902370-C-G

104538991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902358-A-G

http://identifiers.org/hco/4/GRCh38#104538994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133902349-C-A

104539118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902220-T-C

104539118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902220-T-G

104539312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902025-T-G

104539320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902018-G-A

http://identifiers.org/hco/4/GRCh38#104539648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133901730-C-A

104543519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901282-T-C

104543663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901147-A-G

http://identifiers.org/hco/4/GRCh38#104543708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133901117-C-A

104544107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900734-C-T

104544556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900298-A-G

104544688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900153-C-G

104544688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900153-C-T

104544695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900146-C-G

http://identifiers.org/hco/4/GRCh38#104544708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133900141-A-C

http://identifiers.org/hco/4/GRCh38#104544749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133900104-C-A

104544776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900080-A-G

104544913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899988-C-T

104544935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899977-T-G

104544988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899930-T-C

104545206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899722-T-C

104545209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899719-T-C

104545209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899719-T-G

104545295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899611-T-C

104545756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899143-G-A

http://identifiers.org/hco/4/GRCh38#104545878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133899020-A-C

http://identifiers.org/hco/4/GRCh38#104546595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133898338-A-C

104546602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898331-G-A

104546642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898273-T-C

104546724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898193-A-T

104547555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896903-A-G

104547897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896601-A-G

104548734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896025-C-T

104548743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896016-C-T

104548864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133895895-T-C

104549511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133895195-C-G

104549511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133895195-C-T

104549530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133895176-G-A

http://identifiers.org/hco/4/GRCh38#104549694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133894977-C-A

104549694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894977-C-G

104549695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894976-T-G

http://identifiers.org/hco/4/GRCh38#104550304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133894243-C-A

104550457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894121-A-G

104550621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893961-G-A

104550674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893901-A-G

104550988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893028-G-A

http://identifiers.org/hco/4/GRCh38#104551042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133892974-A-C

104551141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892896-A-T

http://identifiers.org/hco/4/GRCh38#104551726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133892341-C-A

104551864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892204-C-T

104552514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133891483-T-C

104552651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133891349-T-C

104553399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890326-C-G

104553556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890181-A-T

http://identifiers.org/hco/4/GRCh38#104553590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133890136-C-A

104553590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890136-C-G

104553654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133890071-A-G

104554004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889623-T-C

104554172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889477-C-T

104555226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889034-A-G

104555343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888915-T-C

104555471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888809-C-T

104556082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888251-C-T

104556604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133886445-T-C

104556699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133886354-A-T

104556719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133886334-T-C

104556831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133886206-T-C

104557101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133885754-G-A

104557246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133885615-T-G

http://identifiers.org/hco/4/GRCh38#104557739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133884931-A-C

104557739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884931-A-T

104557756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884914-A-G

104557841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884829-G-C

104557961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884708-G-A

104557961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884708-G-T

104557965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884704-G-A

104557965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884704-G-C

http://identifiers.org/hco/4/GRCh38#104557969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133884700-C-A

104558186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884484-C-G

104558504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133884174-A-G

104558990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133883738-T-C

104559422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133881717-G-A

104559698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133881486-T-C

104559739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133881449-G-A

104559896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133881300-C-T

http://identifiers.org/hco/4/GRCh38#104559897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133881299-C-A

104560767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133881002-A-G

104561373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879904-G-A

104561442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879837-A-G

104561485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879808-T-C

104561566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879724-T-C

104561671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879617-C-T

104561749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879538-T-C

104569052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878572-A-G

104569143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878483-G-T

104569550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878241-A-G

104569731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878093-T-A

104570830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876790-T-C

http://identifiers.org/hco/4/GRCh38#104570840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133876780-A-C

104570840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876780-A-G

104570909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876713-C-T

104571091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876548-G-C

104571117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876520-T-G

104571422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876236-A-G

104572140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875743-G-A

104572158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875725-T-C

104572236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875647-C-G

104572248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875634-T-C

104572544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875379-A-G

104572658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133875277-G-C

104573923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873861-T-C

104574033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873745-T-A

104574154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873647-C-T

104574454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873361-A-G

104574631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873187-A-G

104574857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872968-A-G

104574907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872914-A-T

104575007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872425-C-T

104575143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871065-G-A

104575322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870847-T-C

104575358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870786-T-C

104575602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870442-T-C

http://identifiers.org/hco/4/GRCh38#104576057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133869695-C-A

104576057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869695-C-T

104576087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869665-G-A

104576207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869555-T-G

104576333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869418-T-G

104576377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869375-G-T

104576573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869209-C-T

http://identifiers.org/hco/4/GRCh38#104576585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133869197-A-C

104576585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869197-A-G

104576942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133868821-A-G

104577395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133868422-C-T

104577443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133868379-G-A

http://identifiers.org/hco/4/GRCh38#104586444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133858808-A-C

104586487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858773-T-C

104586504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858754-G-T

104586514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858744-T-C

104586695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858575-C-T

104586752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858523-T-G

http://identifiers.org/hco/4/GRCh38#104586861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133858436-C-A

http://identifiers.org/hco/4/GRCh38#104586889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133858406-A-C

104586889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858406-A-T

104587234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858309-T-C

104587298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133858245-G-C

104590532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853757-A-G

104590718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853604-T-C

104590922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853469-G-A

104590987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853394-T-C

104591058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853323-A-T

104591075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853306-C-T

104591121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853255-T-C

104591705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852621-G-C

104591963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852356-T-A

http://identifiers.org/hco/4/GRCh38#104592177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133852144-C-A

104592261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852060-A-T

104592539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851772-G-A

104592591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851711-C-T

104592705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851594-C-G

104592939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851351-C-T

104593133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851167-G-A

104593334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850965-T-C

104593712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850625-A-G

104593820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850401-A-G

104593855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850318-A-G

104593977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850063-A-G

104594016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850015-C-T

104594539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849525-A-G

104594598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849464-T-C

104594701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849362-G-A

104594712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849351-A-G

104594728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849335-G-A

104594728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849335-G-C

http://identifiers.org/hco/4/GRCh38#104595126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133849135-A-C

104595500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848916-A-G

104595615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848803-A-G

104595652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848767-G-A

104595674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848744-G-A

http://identifiers.org/hco/4/GRCh38#104595744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133848674-C-A

104595744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848674-C-T

104607697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133842603-C-T

104607734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133842567-T-C

104608734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133841513-T-C

104618977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840646-A-G

104619017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840606-A-G

104619219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840436-A-G

104619894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839797-G-C

104620108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133838826-G-A

104620191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133838745-A-G

104624199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133838211-T-C

104624199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133838211-T-G

http://identifiers.org/hco/4/GRCh38#104624233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133838179-A-C

104624299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133838117-T-C

104624493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837935-A-G

104624733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837746-A-G

104624813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837663-T-C

104624980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837490-G-C

104625005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837464-A-G

104625091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837379-T-A

http://identifiers.org/hco/4/GRCh38#104625215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133837211-A-C

http://identifiers.org/hco/4/GRCh38#104625349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133837081-C-A

http://identifiers.org/hco/4/GRCh38#104625413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133837018-C-A

104625492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836933-C-T

104627109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836746-G-A

104627158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836702-T-C

104627257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836600-G-C

104627310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836533-A-G

104627609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836252-C-G

104627831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836046-G-T

104628011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835868-T-G

104628177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835470-A-G

104628254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835391-T-G

104628327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835317-C-T

104628870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834364-G-T

http://identifiers.org/hco/4/GRCh38#104628910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133834328-C-A

104628910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834328-C-T

104628917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834321-G-A

104628917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834321-G-T

http://identifiers.org/hco/4/GRCh38#104628941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133834300-C-A

104629030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834183-T-C

104629109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834115-G-A

104629224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834002-T-C

http://identifiers.org/hco/4/GRCh38#104629507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133833757-A-C

104629568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833696-T-G

104629654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833429-G-C

104629654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833429-G-T

104629754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833274-A-T

104629861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833184-A-G

http://identifiers.org/hco/4/GRCh38#104630781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133831538-C-A

104630838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133831492-T-C

104630924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133831407-T-C

http://identifiers.org/hco/4/GRCh38#104630946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133831385-C-A

104630952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133831379-T-C

104631245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133831104-C-T

http://identifiers.org/hco/4/GRCh38#104632621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133830953-C-A

104633354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133830296-T-G

104633505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133829135-G-A

104634071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133828613-A-T

104634077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133828601-G-A

104634431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133828324-T-C

104634712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133828063-G-A

104635018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827614-T-C

http://identifiers.org/hco/4/GRCh38#104635594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133827387-C-A

104635594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827387-C-T

104635671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827331-C-T

104635806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827230-C-G

104635893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827146-C-G

104635951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133827095-A-G

http://identifiers.org/hco/4/GRCh38#104636564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133824558-C-A

104636772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133824271-T-C

104636824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133824187-T-C

http://identifiers.org/hco/4/GRCh38#104636841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133824164-C-A

104636841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133824164-C-T

104637018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133823902-T-C

104637176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133823738-G-C

104637365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133823516-C-G

104637489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133823411-T-C

104637564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133822876-A-T

104637579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133822861-T-C

104637588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133822852-T-C

104639746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133822168-T-C

http://identifiers.org/hco/4/GRCh38#104639811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133822113-A-C

104639811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133822113-A-G

http://identifiers.org/hco/4/GRCh38#104640044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133822017-A-C

104640078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821983-T-C

104640167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821961-T-C

104640231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821898-T-A

104640252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821877-A-G

104640412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821719-A-G

http://identifiers.org/hco/4/GRCh38#104640519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133821615-A-C

http://identifiers.org/hco/4/GRCh38#104640619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133821527-A-C

104640844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821351-G-A

104640844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821351-G-C

104640909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821286-G-A

http://identifiers.org/hco/4/GRCh38#104640913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133821282-A-C

104640983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821166-T-A

104641042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821046-G-A

104641042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821046-G-C

104641042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133821046-G-T

http://identifiers.org/hco/4/GRCh38#104641052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133821033-A-C

104641142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820941-G-A

104641142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820941-G-T

104641191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820895-T-C

104641230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820853-T-C

104641288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820753-A-G

104641304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820737-T-C

104641641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820420-C-T

104641674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820387-A-T

104641675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820386-C-G

104641705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820356-C-T

104641881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820200-G-C

104642107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133820002-T-C

104642533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133819663-A-G

104642546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133819650-G-A

104642589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133819605-T-C

http://identifiers.org/hco/4/GRCh38#104642749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133819445-C-A

104658641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133818803-T-C

104658644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133818800-G-A

104658879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133818550-G-T

104659012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133818443-T-G

104660209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133817516-G-A

104660271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133817456-A-G

104660316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133817396-C-T

104660379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133817337-G-A

http://identifiers.org/hco/4/GRCh38#104660749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133816489-A-C

104660752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133816486-T-C

http://identifiers.org/hco/4/GRCh38#104660844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133816401-C-A

104660844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133816401-C-T

104660933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133816314-C-T

104661075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133816191-G-A

104661466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133815206-A-G

104661602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133815081-T-C

104661603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133815080-T-C

104661973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133814540-G-C

104662200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133814329-G-C

104662457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133814089-G-T

http://identifiers.org/hco/4/GRCh38#104664865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133811734-C-A

http://identifiers.org/hco/4/GRCh38#104664959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133811641-A-C

104665013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811597-G-A

104665013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811597-G-C

104665013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811597-G-T

104665193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811418-T-G

104665360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811244-C-G

104665363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133811241-A-G

104666005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133810609-T-A

104666441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133810216-C-T

104669437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809794-G-A

104669437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809794-G-T

104669551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809667-G-A

104669665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809558-C-G

http://identifiers.org/hco/4/GRCh38#104669674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133809549-A-C

104669976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809249-T-G

104670151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133809086-G-T

104670272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133808959-G-C

104670513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133808698-A-T

104675264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133808079-C-T

104675524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133807802-G-A

104675537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133807789-A-T

104676029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133807108-C-T

104676076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133807060-T-G

104676087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133807049-A-T

104676262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806876-G-A

104676262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806876-G-T

104676307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806831-T-C

http://identifiers.org/hco/4/GRCh38#104676409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133806744-A-C

104676500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806678-C-T

104676527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806651-A-G

104676528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806650-C-T

104676551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806446-A-G

104676619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806364-A-G

104676791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806198-A-G

104676833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133806175-C-T

104677270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805727-G-C

104677349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805651-T-G

104677495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805498-T-C

104677609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805388-G-T

104677709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805252-T-C

104677782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133805172-G-A

104678496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133804499-A-G

104678766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133804230-A-G

104679187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133803483-G-A

104679187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133803483-G-T

104679645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133802133-T-G

104679727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133802051-T-C

104679876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133801895-G-A

104680450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133801321-T-A

104685047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133791227-C-T

http://identifiers.org/hco/4/GRCh38#104685186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133791076-C-A

104685651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133790535-T-G

104685875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133790329-T-A

http://identifiers.org/hco/4/GRCh38#104686194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133790048-A-C

104686194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133790048-A-T

104686242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133790007-T-C

104686271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789984-T-G

104686630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789615-T-C

104686630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789615-T-G

104686892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789348-G-C

104686892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789348-G-T

104693083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789056-T-A

104693083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789056-T-C

104693086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133789053-T-C

104693140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133788999-T-A

104693403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133788776-G-A

104693410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133788769-G-A

104694636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133788326-G-T

104694735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133788165-G-A

104694939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787439-A-G

104694957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787423-T-C

104695085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787302-T-A

104695092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787295-G-A

104695094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787293-T-C

104695262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133787130-T-C

104695564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133786475-T-A

104695734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133786300-G-A

104695734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133786300-G-T

104695967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133786104-T-G

104696232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133785851-C-T

104696656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133785323-T-A

104697145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133785120-T-C

104697761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133784478-C-T

104698049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133783570-T-C

104698113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133783363-T-C

104698272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133783184-T-A

104698501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133782948-T-G

104698805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133782681-A-G

104699207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133782255-T-C

104699300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133781991-G-T

http://identifiers.org/hco/4/GRCh38#104699564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133781732-A-C

104699564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133781732-A-G

104699736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133781567-A-G

104700001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133781330-A-G

104700812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133780853-T-C

http://identifiers.org/hco/4/GRCh38#104701115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133780242-A-C

104701237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133780117-T-C

104701320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133780027-A-G

104702694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133761802-T-C

104703032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133761485-T-C

104703998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133758167-T-A

104704154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133758038-G-C

104704415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757788-C-G

104704538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757670-G-A

104704923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757321-T-C

104704994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757249-T-C

104705010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757233-T-C

104705014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757229-G-A

104705071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133757165-T-C

104705329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133756987-C-T

104705619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133756702-A-G

104706172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133756185-T-G

http://identifiers.org/hco/4/GRCh38#104706485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133755906-A-C

http://identifiers.org/hco/4/GRCh38#104713311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133755091-C-A

104713451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754960-C-T

104713491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754923-G-C

104713691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754723-C-T

104714131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754311-C-G

104714131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754311-C-T

104714144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133754298-A-G

104714512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133753919-G-A

104714716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133753079-A-T

104714824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133752992-A-G

104714824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133752992-A-T

104715162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133750431-T-A

104715220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133750378-A-G

104715300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133750297-G-C

104715329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133750268-C-T

104715558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133750063-A-G

104715665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749969-C-T

104715667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749967-G-T

104715740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749895-T-C

104715744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749891-T-C

104715878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749760-C-T

104715978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133749656-T-C

104725109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133743260-A-G

104725217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133743163-A-G

104725371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133743017-G-A

104725373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133743015-A-G

104725396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742988-T-C

104725865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742858-C-G

104726079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742654-T-C

104726169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742574-A-G

104726479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742289-A-G

104726643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133742124-T-G

104726719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133741599-A-G

104726764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133741558-G-C

104727116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133741220-C-T

104727349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133740991-C-T

104727412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133740924-T-C

104727499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133740848-G-A

104727536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133740818-G-A

104727572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133740803-C-T

104727711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 133740725-G-A

104727711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 133740725-G-T

104727735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133740701-C-T

104728042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133740399-G-A

http://identifiers.org/hco/4/GRCh38#104728123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133740299-C-A

104728123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133740299-C-T

104728211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133740219-T-C

104728303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133740127-G-A

104728504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133739928-T-A

http://identifiers.org/hco/4/GRCh38#104728505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#133739927-C-A

104728539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133739923-A-G

104728797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133739649-T-A

104728815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133739630-G-C

104728817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133739628-A-G

104729412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737873-T-G

104729829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737576-A-T

104731097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737337-T-C

104731484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737255-C-T

104731507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737232-A-G

104731704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737039-G-A

104731707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133737036-T-C

104731818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133736923-C-G

104731854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133736900-T-G

http://identifiers.org/hco/4/GRCh38#104732236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133729403-A-C

104732454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729220-T-A

104732571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729121-T-A

104732604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729088-G-A

104732636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729061-G-A

104732636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729061-G-C

104732670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133729041-C-T

104732756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133728955-C-G

104734538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41054
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133724763-G-C