84748697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron_variant, undefined
orthologous variants: 80643543-G-A

84748921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80643741-C-T

84749032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 80643835-C-T

84749092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 80643895-C-T

84749189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80643992-C-T

84749514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80644336-G-A

84749597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80644416-C-G

84749657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80644467-A-G

84749763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80644545-G-A

84750646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron_variant, undefined
orthologous variants: 80645398-A-G

84751222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80646009-A-G

84751343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80646115-G-T

84752359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80647064-C-G

84752555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80647361-T-C

84753623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80648718-C-T

84755257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80649612-C-G

84755294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80649645-T-C

84755498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80649759-C-T

84755517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80649778-A-T

84755551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80649810-C-T

84755792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80650036-A-G

http://identifiers.org/hco/15/GRCh38#84756041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80650546-C-A

84756041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80650546-C-T

84756335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80650835-G-C

84756468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80650932-A-G

84756603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80651029-A-G

84756624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80651050-C-T

84756625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80651051-C-T

84759148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80651792-A-G

84759148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80651792-A-T

http://identifiers.org/hco/15/GRCh38#84759377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80652010-C-A

84759431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80652058-G-A

84759483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80652134-C-G

84759497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80652148-G-A

84760388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654016-A-G

84760583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654168-G-A

84760773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654330-G-A

84760817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654371-G-C

84760817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654371-G-T

84760884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654430-G-A

84761343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654592-A-G

84761353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654602-A-G

84761411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654658-A-T

84761555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654784-G-A

84761699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80654895-G-A

84761831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80655018-A-G

84761886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80655071-C-G

84762140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80655234-G-A

84762229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80655322-T-C

84762402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80656357-G-C

84762414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80656369-C-T

84762449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80656404-A-G

84762641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80656542-C-T

84763280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80657141-G-A

84763304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80657167-A-G

84763546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80657362-G-T

84764606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659067-A-G

84764671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659146-C-G

84764759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5 prime UTR variant
orthologous variants: 80659231-G-A

84764759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5 prime UTR variant
orthologous variants: 80659231-G-C

84764759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 5 prime UTR variant
orthologous variants: 80659231-G-T

84764835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659307-C-G

84765009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659453-C-T

84765036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659473-C-T

84765038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80659475-C-T

84765547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660111-T-G

84765548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660112-T-G

84765860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660425-A-G

84765883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660463-C-T

84766091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660723-G-A

84766143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660769-A-G

84766180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80660854-A-G

84767471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80663055-G-C

84768781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80663874-T-G

84769001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80664275-C-T

84769122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80664404-G-C

http://identifiers.org/hco/15/GRCh38#84769126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80664408-A-C

84769653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80664673-G-A

84770081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80664881-C-G

84770159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80664962-G-T

http://identifiers.org/hco/15/GRCh38#84770194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80665030-A-C

84770508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80665303-T-G

84770669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80665419-G-A

84771745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80665894-C-G

84771745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80665894-C-T

84774710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80668920-G-A

84774737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80668937-A-G

84775243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80669363-C-T

84775386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80669488-G-A

84775582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80669632-A-G

84775712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: intron variant
orthologous variants: 80669744-G-A

84780735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80671470-C-T

84782557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80672907-G-A

84782557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80672907-G-T

84782566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80672916-G-A

84782566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80672916-G-T

http://identifiers.org/hco/15/GRCh38#84782693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80673055-C-A

84782693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80673055-C-G

84782732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80673094-A-G

84783056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80673418-G-A

http://identifiers.org/hco/15/GRCh38#84783084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80673446-A-C

84783174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80673536-A-G

84783176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80673538-T-A

84783206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80673562-T-C

84783516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80673872-C-T

84783677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674033-C-T

84783704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674060-C-G

84783821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674177-A-G

84783821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674177-A-T

84783830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674186-G-A

84783851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674207-A-G

84783869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674225-T-C

84783987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674352-A-T

84784074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674439-C-T

84784077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674442-C-G

84784077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674442-C-T

84784157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674519-C-G

84784157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674519-C-T

84784203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80674565-C-T

84784499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674861-G-A

84784499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80674861-G-T

84784703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80675065-C-G

84784703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80675065-C-T

84784820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80675182-A-G

84785493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80675694-G-C

84785724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80675860-G-A

84785740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80675876-A-G

84785749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80675885-G-T

84785761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80675897-G-A

84787361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80677918-C-T

84787514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80678059-C-T

84790664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80679156-A-G

84790664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80679156-A-T

84790672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80679164-T-G

84790743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80679235-C-T

84790746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80679238-T-C

84790806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80679298-G-C

84790806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80679298-G-T

http://identifiers.org/hco/15/GRCh38#84793115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80684100-C-A

84793115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80684100-C-T

84793181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80684156-A-G

84794990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80684713-C-G

84795192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80685854-A-T

http://identifiers.org/hco/15/GRCh38#84795237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80685883-A-C

84795237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80685883-A-G

84797846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687072-C-T

84797848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687074-C-T

84797881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 80687110-T-C

84798257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687481-G-A

http://identifiers.org/hco/15/GRCh38#84798408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80687646-C-A

84798408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80687646-C-T

84798514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687738-A-G

84798514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687738-A-T

http://identifiers.org/hco/15/GRCh38#84798560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80687784-A-C

84798560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80687784-A-G

84798776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80688000-G-T

84798812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80688036-G-A

84798942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688167-C-T

84798989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688214-G-T

84799022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688243-G-A

84799022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688243-G-T

84799201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80688404-A-G

http://identifiers.org/hco/15/GRCh38#84799256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80688457-C-A

84799352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688533-G-T

84799429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80688606-C-T

84799941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80688977-G-A

84799941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80688977-G-T

84800055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80689102-G-C

http://identifiers.org/hco/15/GRCh38#84800075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80689122-A-C

84800075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80689122-A-G

84800110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80689146-A-G

84800482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80689638-C-G

84800482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80689638-C-T

84800886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690047-T-G

84800893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690054-T-C

84800907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690068-T-A

84800907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690068-T-C

84800920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690081-C-T

http://identifiers.org/hco/15/GRCh38#84801723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80690946-C-A

84801765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80690999-G-A

84801883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80691116-A-G

84802141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80691374-G-A

84802141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80691374-G-T

84802309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80691527-T-G

84802434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80691643-A-G

84802616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80691824-G-A

84802616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80691824-G-T

84802642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80691850-A-G

http://identifiers.org/hco/15/GRCh38#84802651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80691859-C-A

84802651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80691859-C-T

http://identifiers.org/hco/15/GRCh38#84802685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80691893-C-A

84802949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692128-T-A

84802949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692128-T-C

84802955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692134-T-C

http://identifiers.org/hco/15/GRCh38#84803385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80692549-C-A

84803385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692549-C-G

84803385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692549-C-T

84803403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692565-A-G

84803403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692565-A-T

http://identifiers.org/hco/15/GRCh38#84803407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80692569-C-A

84803421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692583-A-G

84803507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692663-G-T

84803518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692675-G-A

84803663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692804-G-T

84803728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692849-T-A

84803728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80692849-T-C

http://identifiers.org/hco/15/GRCh38#84803763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80692884-C-A

84803763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80692884-C-T

84803767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80692888-G-A

84803767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80692888-G-T

84803875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80692939-G-A

84803879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80692943-G-A

84803879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80692943-G-C

84803910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80692961-A-T

84804016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693063-T-C

http://identifiers.org/hco/15/GRCh38#84804189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80693241-C-A

http://identifiers.org/hco/15/GRCh38#84804193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80693245-C-A

84804193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693245-C-T

84804221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693260-C-T

http://identifiers.org/hco/15/GRCh38#84804250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80693289-C-A

84804250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693289-C-T

84804307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693402-A-G

84804319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693414-G-T

84804353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80693438-G-T

84804408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80693492-T-C

http://identifiers.org/hco/15/GRCh38#84804872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80693887-C-A

84804872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80693887-C-T

84805060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80694063-T-C

84805268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80694238-T-A

84805268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80694238-T-C

http://identifiers.org/hco/15/GRCh38#84805302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80694270-C-A

84805354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80694311-G-A

84805354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80694311-G-T

84806125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80695035-T-G

http://identifiers.org/hco/15/GRCh38#84806266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#80695175-C-A

84806266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28986
most severe consequence: 3 prime UTR variant
orthologous variants: 80695175-C-T