http://identifiers.org/hco/7/GRCh38#104738982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23310052-C-A

104739027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310095-A-G

104739027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310095-A-T

http://identifiers.org/hco/7/GRCh38#104739147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23310198-C-A

104739148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310199-A-G

http://identifiers.org/hco/7/GRCh38#104739211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23310261-C-A

http://identifiers.org/hco/7/GRCh38#104739223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23310273-A-C

104739226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310276-T-C

104739359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310404-T-C

104739506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310426-G-A

104739664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310544-A-T

104739772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310671-G-A

http://identifiers.org/hco/7/GRCh38#104739785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23310681-A-C

104739793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310689-T-C

104739897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23310778-G-T

104740916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311028-C-T

104740962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311075-G-C

104741033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311138-G-C

104741041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311146-G-A

104741121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311223-T-C

104741281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311386-A-G

104741363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311504-G-T

104741381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311520-T-G

http://identifiers.org/hco/7/GRCh38#104741422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23311540-C-A

104741449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311567-A-T

104741544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311596-T-C

104741560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23311612-G-T

104742446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312241-A-G

104742473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312264-G-A

104742597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312371-T-A

http://identifiers.org/hco/7/GRCh38#104743200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23312627-A-C

104743200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312627-A-G

104743235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312661-C-T

104743236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312662-A-G

104743284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312709-A-G

104743360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312781-A-G

http://identifiers.org/hco/7/GRCh38#104743452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23312857-C-A

104743463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312868-C-T

104743615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23312989-C-G

104744512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23313542-G-C

http://identifiers.org/hco/7/GRCh38#104747229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23322337-C-A

104747236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23322343-C-T

104747640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23322727-C-T

104753261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23323628-C-T

104753402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23323807-T-C

104753665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23324060-T-C

http://identifiers.org/hco/7/GRCh38#104753956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23324357-C-A

104754113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23324484-G-A

104756335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23324833-A-G

104756436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23324937-G-T

104756470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23324970-A-G

104758678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23325370-C-G

104758678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23325370-C-T

104759159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23325836-G-A

104759222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23325897-T-C

104759472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329446-T-A

104759524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329492-T-C

http://identifiers.org/hco/7/GRCh38#104759525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23329493-A-C

104759584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329528-G-A

104759587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329531-A-G

104759853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329776-C-T

104759860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329783-G-C

104759860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329783-G-T

104759965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329886-A-G

104760050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23329970-A-G

104760784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23330694-G-C

104760839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23330749-C-G

104760839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23330749-C-T

104761126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23331070-G-A

104761127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23331071-G-A

104761127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23331071-G-T

104761241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23331305-C-G

104761263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23331327-A-G

104761445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332248-C-T

104761903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332685-A-G

104762141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332882-A-G

104762155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332896-G-A

104762326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332933-G-C

104762326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332933-G-T

104762350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332955-T-A

104762404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23332996-C-G

104763006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335095-A-G

104763082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335169-C-G

104763082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335169-C-T

104763450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335591-A-G

104763457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335598-T-C

104763477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335617-G-T

104763572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23335724-G-A

http://identifiers.org/hco/7/GRCh38#104764068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23337524-C-A

104764099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23337555-A-T

104764138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23337594-C-G

104764756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23337838-T-C

104764803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23337884-A-G

104764815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23337896-A-G

104765217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23338305-G-A

104765419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23338499-T-A

104765698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23338773-C-T

104766228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339497-A-G

104766624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339792-C-T

104766631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339799-G-A

104766715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339865-A-G

104766719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339869-T-G

104766761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339914-C-G

104766813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23339963-A-G

104768136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340060-T-A

104768136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340060-T-C

104768286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340433-T-C

104768367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340512-A-G

104768494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340633-T-C

http://identifiers.org/hco/7/GRCh38#104768538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23340672-C-A

104768573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340693-A-G

104768634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340751-T-C

104768637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340754-G-A

104768637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340754-G-T

104768923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23340989-C-T

104768974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23341030-T-C

104769000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23341056-A-G

104770440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23341830-A-G

104770554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23341914-C-T

104770583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23341943-T-G

104770774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23342143-T-C

http://identifiers.org/hco/7/GRCh38#104770793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23342166-A-C

104772487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345130-C-T

104772549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345172-T-C

104772554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345177-C-T

http://identifiers.org/hco/7/GRCh38#104772620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23345238-A-C

104772770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345375-A-G

104772902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345507-T-A

104772907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345512-G-A

104773255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345827-G-A

http://identifiers.org/hco/7/GRCh38#104773842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23346583-C-A

104774153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23346869-T-C

104774183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23346900-G-A

http://identifiers.org/hco/7/GRCh38#104774619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23347239-A-C

104774806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23347414-A-G

104775081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23347667-C-T

104775419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23347710-C-G

104775876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23348124-A-G

104775876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23348124-A-T

104775966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23348208-G-T

104775970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23348212-T-C

104776737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23349595-T-C

104776832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23349667-A-G

104777217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23349996-T-C

104777260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350039-G-A

104777260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350039-G-C

104777376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350153-G-A

104777637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350332-T-C

104778030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350672-G-A

104778096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350757-C-T

104778104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350765-G-A

104778104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23350765-G-C

104778297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23351088-A-G

104780284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23351704-C-T

104780443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23351862-G-A

104780443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23351862-G-C

104780762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352038-A-G

104780808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352083-C-T

http://identifiers.org/hco/7/GRCh38#104780855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23352129-A-C

104781059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352327-G-C

104781185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352446-C-T

104781609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353083-T-G

104781901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353309-G-C

104781901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353309-G-T

104782124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353507-G-C

104782364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353704-G-A

104782410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353723-G-A

104782410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353723-G-T

104782593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353863-G-C

104782817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354065-T-C

104783396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354775-G-A

104783396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354775-G-C

104783458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354838-A-G

104783555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354928-C-T

104783556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23354929-G-A

104784645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356067-T-G

104784702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356157-C-T

104784748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356255-C-T

104784838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356350-T-G

104784933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356431-T-C

http://identifiers.org/hco/7/GRCh38#104784974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23356473-A-C

104785214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356667-A-T

104785230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356683-T-C

104785247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356700-T-A

104785247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356700-T-C

http://identifiers.org/hco/7/GRCh38#104785265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23356718-C-A

104785265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356718-C-T

104785415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356842-G-T

104785558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23356975-G-A

104785644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23357066-G-T

104785769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23357184-G-A

104785769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23357184-G-C

104785911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23357280-T-C

http://identifiers.org/hco/7/GRCh38#104786150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23357439-C-A

104786409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23357674-T-C

104786825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23358049-A-G

104786840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23358064-T-C

104787369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360182-C-T

104787512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360325-T-C

http://identifiers.org/hco/7/GRCh38#104787520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23360332-C-A

104787529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360341-A-G

104787547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360355-A-G

104787870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360414-G-T

104788013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360537-T-C

104788060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360554-G-C

http://identifiers.org/hco/7/GRCh38#104788100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23360592-A-C

104788120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360612-G-A

104788121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360613-C-G

104788121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360613-C-T

104788192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23360683-T-C

104788635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361075-G-T

http://identifiers.org/hco/7/GRCh38#104788835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23361285-C-A

104788835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361285-C-T

104788945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361337-A-G

104789107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361498-G-A

104789318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361740-G-A

104789323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361745-C-G

104789335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361757-T-C

104789371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361807-G-A

104789371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23361807-G-T

104789557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23364812-T-C

104789848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365075-A-G

104789884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365107-A-T

104789912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365133-A-G

104789956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365166-A-G

104789965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365175-T-C

104790174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365373-C-T

http://identifiers.org/hco/7/GRCh38#104790228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23365429-C-A

104790281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365480-T-C

104790712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365848-T-G

104791298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23366539-T-G

104791494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23366726-G-C

104791496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23366728-T-C

104791781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23367164-G-A

104791781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23367164-G-C

104791782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23367165-T-C

104792002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23367725-A-G

104792106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23367828-T-G

104792365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23368074-A-G

104792454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23368156-T-C

104792747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23368429-C-G

104792753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23368435-C-T

104793235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23369014-C-T

104793335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23369117-G-A

104793371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23369150-G-T

104793504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23369283-G-T

104793709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23369524-C-T

104794309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370007-G-A

http://identifiers.org/hco/7/GRCh38#104794386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23370083-C-A

104794437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370124-C-T

104794789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370460-G-A

104794850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370529-G-A

104794854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370533-A-G

104795008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370706-G-T

104795088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370786-A-G

104795125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370824-G-A

104795125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23370824-G-T

104795352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371050-A-T

104795499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371186-A-T

104795809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371501-C-T

104795868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371561-T-A

104795868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371561-T-C

104796068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371755-C-T

104796131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371817-A-G

104796286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23371963-G-A

104796537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372204-G-T

104796544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372211-G-C

http://identifiers.org/hco/7/GRCh38#104796611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23372279-C-A

104796630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372296-A-T

104796821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372436-T-C

http://identifiers.org/hco/7/GRCh38#104796829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23372444-C-A

104796829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372444-C-T

http://identifiers.org/hco/7/GRCh38#104796950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23372582-C-A

104796965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372597-G-T

104796999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372630-G-T

104797139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23372758-T-C

104798453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23375650-T-C

104798864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378188-G-C

104799027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378339-G-A

http://identifiers.org/hco/7/GRCh38#104799042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23378354-C-A

104799263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378581-T-C

104799287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378614-G-A

http://identifiers.org/hco/7/GRCh38#104799304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23378631-C-A

104799304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378631-C-T

104799305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378632-T-C

104799345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378651-G-A

104799345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378651-G-T

104799417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378706-C-T

104799489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378771-G-A

104799489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378771-G-T

104799675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378929-A-G

104799679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378933-A-G

104799693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378946-G-A

104799709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378962-C-T

104799720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378973-G-T

104799726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23378979-A-T

104799760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379014-A-G

http://identifiers.org/hco/7/GRCh38#104799769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23379023-C-A

104799783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379037-T-A

http://identifiers.org/hco/7/GRCh38#104799822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23379076-A-C

104799822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379076-A-G

104799822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379076-A-T

104799850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379104-A-G

104799888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379143-G-A

http://identifiers.org/hco/7/GRCh38#104799964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23379220-C-A

104800049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379303-C-T

104800093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379345-G-T

http://identifiers.org/hco/7/GRCh38#104800396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23379734-A-C

104800396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379734-A-T

104800547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23379834-C-T

104801404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23380650-T-A

http://identifiers.org/hco/7/GRCh38#104801451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23380702-C-A

104801988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381442-G-A

104801997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381452-C-T

104802186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381566-G-A

104802696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381732-G-T

http://identifiers.org/hco/7/GRCh38#104802705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23381742-C-A

104802705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381742-C-T

104802768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23381792-T-C

http://identifiers.org/hco/7/GRCh38#104802775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23381799-C-A

104802841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 23381856-G-T

104803451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 23382210-C-T

104803479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23382238-G-T

104803501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23382258-T-C

104803507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23382264-T-C

104803566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23382320-A-G

http://identifiers.org/hco/7/GRCh38#104803960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23387305-C-A

http://identifiers.org/hco/7/GRCh38#104803992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#23387336-A-C

104804030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23387371-T-C

104804053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23387396-A-G