106298043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84408509-G-A

106300887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84410867-T-G

106301792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411896-C-T

106301983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412087-G-A

106302010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412115-G-A

106302010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412115-G-C

106302083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412186-G-T

106302115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412218-G-A

106302115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412218-G-T

http://identifiers.org/hco/12/GRCh38#106302407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412383-A-C

106302407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412383-A-G

106302469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412427-G-A

106302476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412434-C-T

106302501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412458-G-A

106302550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412506-G-A

106302556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412512-G-A

106302600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412556-T-C

106302664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412620-G-A

106302664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412620-G-T

106302668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412624-G-A

106302668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412624-G-T

http://identifiers.org/hco/12/GRCh38#106302711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412667-C-A

106302711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412667-C-T

http://identifiers.org/hco/12/GRCh38#106302791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412735-A-C

106302791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412735-A-G

106302824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412764-T-C

106302824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412764-T-G

http://identifiers.org/hco/12/GRCh38#106302853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412792-C-A

106302853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412792-C-T

106302886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412825-G-T

106302983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84412918-G-A

http://identifiers.org/hco/12/GRCh38#106302986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412921-C-A

106302986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412921-C-T

http://identifiers.org/hco/12/GRCh38#106303011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84412931-C-A

106303011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412931-C-T

106303134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84412983-G-A

106303230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413047-C-T

106303365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413190-G-A

106303480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413303-G-A

106303480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413303-G-T

http://identifiers.org/hco/12/GRCh38#106303482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84413305-C-A

106303482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413305-C-T

106303491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413314-G-A

106303491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413314-G-C

106303491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413314-G-T

106303497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84413320-G-T

106303507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413328-A-T

106303807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413681-C-T

http://identifiers.org/hco/12/GRCh38#106303953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84413811-C-A

106304001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413850-G-A

106304001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413850-G-C

106304008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84413863-T-A

http://identifiers.org/hco/12/GRCh38#106304062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84413922-C-A

106304064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84413924-T-C

106304177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414021-A-G

http://identifiers.org/hco/12/GRCh38#106304182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84414026-C-A

106304182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414026-C-T

106304216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414035-A-G

106304218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414037-A-G

106304224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414043-A-G

106304224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84414043-A-T

106304269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84414093-T-C

106304334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 84414156-A-G

106304557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414329-A-G

106304557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414329-A-T

106304565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414337-C-T

106304887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414657-G-A

106304934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414704-C-G

106305125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414900-T-G

106305131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414906-C-T

106305152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84414927-T-G

106305618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84415360-G-A

106305650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84415391-C-G

106306922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84416537-A-G

http://identifiers.org/hco/12/GRCh38#106307041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84416656-C-A

106307291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84416888-A-G

106307339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84416928-C-T

106307375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84416959-G-T

106307415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84416999-G-A

106307415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84416999-G-T

106307449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417033-G-A

106307505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417086-G-T

106307596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417165-T-A

106307698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417259-C-T

106307745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417309-T-C

http://identifiers.org/hco/12/GRCh38#106307794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84417354-A-C

http://identifiers.org/hco/12/GRCh38#106308041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84417569-C-A

106308041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417569-C-T

106308050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417578-T-C

106308255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84417792-T-C

106308559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84418114-G-A

106309306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84418913-G-C

106309385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419016-A-T

106309405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419036-C-T

106309545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419163-C-G

106309702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419311-A-G

106309723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419332-A-G

106309862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419437-A-G

106309926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419505-G-T

106310382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419827-A-T

106310410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84419863-C-G

http://identifiers.org/hco/12/GRCh38#106310514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84420149-C-A

106310577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420195-T-C

106310581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420199-G-A

106310667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420271-G-A

http://identifiers.org/hco/12/GRCh38#106310894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84420453-C-A

106310913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 84420472-T-A

106310913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 84420472-T-C

106310913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 84420472-T-G

http://identifiers.org/hco/12/GRCh38#106310930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84420492-C-A

106310930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420492-C-T

106310990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420555-G-A

106310990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420555-G-T

106311012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420577-A-G

106311012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420577-A-T

http://identifiers.org/hco/12/GRCh38#106311046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84420617-A-C

106311046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84420617-A-G

106311048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84420619-C-G

106311048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84420619-C-T

106311050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84420621-T-A

106311050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 84420621-T-C

106311154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 84420841-A-G

106311173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 84420860-A-G

106311240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 84420927-G-A

106311240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 84420927-G-C

106311289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420974-T-C

http://identifiers.org/hco/12/GRCh38#106311309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84420994-C-A

106311309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84420994-C-T

http://identifiers.org/hco/12/GRCh38#106311369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84421056-A-C

106311369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421056-A-G

106311369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421056-A-T

106311897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421767-A-T

106311940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421788-C-G

106311946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421794-G-T

106311947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421795-C-T

106311977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421822-C-T

106311980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421824-T-A

106312033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84421877-A-G

http://identifiers.org/hco/12/GRCh38#106312256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84422044-C-A

106312256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422044-C-G

106312256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422044-C-T

106312975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422244-G-C

106313270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422643-A-G

106314207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422850-G-A

106314207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422850-G-T

http://identifiers.org/hco/12/GRCh38#106314231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84422866-A-C

106314231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422866-A-G

106314231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422866-A-T

106314261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422895-A-G

106314261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422895-A-T

106314299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422927-G-C

106314338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422949-G-A

106314338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 84422949-G-T

106314392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 84423002-A-G

106314479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: synonymous variant
orthologous variants: 84423089-T-C

106314511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423116-G-T

106314514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423119-G-T

106314536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423146-T-C

106314537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423147-G-A

106314537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423147-G-C

106314537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423147-G-T

106314571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423181-G-A

106314571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423181-G-C

106314571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84423181-G-T

106317802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84424634-G-A

106317913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84424737-G-T

106318248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425666-T-C

106318248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425666-T-G

106318317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425723-A-G

http://identifiers.org/hco/12/GRCh38#106318322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84425726-A-C

http://identifiers.org/hco/12/GRCh38#106318334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84425738-A-C

106318334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425738-A-G

106318334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425738-A-T

106318458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: missense variant
orthologous variants: 84425862-C-G

106318458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: synonymous variant
orthologous variants: 84425862-C-T

106318495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425893-C-T

106318496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425894-G-A

106318496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425894-G-T

106318585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84425976-T-C

http://identifiers.org/hco/12/GRCh38#106318605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84425996-C-A

106319375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426166-T-A

106319375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426166-T-C

106319474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426262-A-T

106319485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426273-G-C

http://identifiers.org/hco/12/GRCh38#106319495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84426283-A-C

106319647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426454-A-G

106321297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426802-T-C

http://identifiers.org/hco/12/GRCh38#106321382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84426882-C-A

http://identifiers.org/hco/12/GRCh38#106321384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84426884-C-A

http://identifiers.org/hco/12/GRCh38#106321396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84426896-C-A

106321396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84426896-C-T

106321625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84427091-C-T

106321726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427192-G-A

http://identifiers.org/hco/12/GRCh38#106321755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84427220-C-A

106321755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427220-C-T

106321765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427226-G-A

106321765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427226-G-C

106321798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427255-T-G

http://identifiers.org/hco/12/GRCh38#106321802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84427259-C-A

106321802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427259-C-G

106321844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427299-G-A

http://identifiers.org/hco/12/GRCh38#106321845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84427300-A-C

106321845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427300-A-G

http://identifiers.org/hco/12/GRCh38#106321846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84427301-C-A

http://identifiers.org/hco/12/GRCh38#106321847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84427302-C-A

106321904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427345-G-C

106321908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427349-G-A

106322066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427518-A-G

106322180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427625-A-G

106322187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427632-G-A

106322203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427647-A-G

106322579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427952-C-T

106322626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427996-A-G

106322723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84428096-G-A

106322773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84428146-G-C

106322943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84428293-A-G

106323068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430112-G-A

http://identifiers.org/hco/12/GRCh38#106323387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84430387-C-A

106323387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430387-C-G

106323387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430387-C-T

106323393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430393-G-T

106323428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430432-T-C

http://identifiers.org/hco/12/GRCh38#106323432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84430436-C-A

106323432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84430436-C-T

106323627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84430629-A-G

106323817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84430700-G-T

106323823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84430706-G-T

106323843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84430722-A-G

106323848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84430727-G-T

106323938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 84430826-G-T

http://identifiers.org/hco/12/GRCh38#106323951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84430839-C-A

106324219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84430998-T-C

106324227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431010-A-T

106324248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431031-G-T

106324271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431054-G-A

106324332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431117-G-T

106324350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431136-G-A

106324350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431136-G-C

106324350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431136-G-T

106324408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431191-A-G

106324414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431196-G-A

106324414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431196-G-T

106324417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431199-T-C

106324510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431224-G-A

106324510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431224-G-C

106324516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431230-A-G

106324699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431393-A-G

http://identifiers.org/hco/12/GRCh38#106324710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84431412-A-C

http://identifiers.org/hco/12/GRCh38#106324967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84431630-C-A

106325009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431664-A-T

106325237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431878-C-G

106325237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431878-C-T

106325239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431880-T-C

106325271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431911-G-A

106325271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431911-G-T

106325281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431921-C-G

106325289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431928-G-A

106325289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431928-G-T

106325321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431960-G-A

106325321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431960-G-T

106325424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431989-G-T

106325430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84431994-G-A

http://identifiers.org/hco/12/GRCh38#106325490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84432036-C-A

106325572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84432119-A-G

106325952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432164-A-G

106326012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432210-G-A

http://identifiers.org/hco/12/GRCh38#106326040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84432236-C-A

106326040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432236-C-G

106326041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432237-A-G

http://identifiers.org/hco/12/GRCh38#106326210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84432402-A-C

106326215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432407-C-T

106326232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432424-C-G

106326495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432665-T-C

106326735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432936-A-G

106326748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84432965-G-C

106326815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84433036-A-G

http://identifiers.org/hco/12/GRCh38#106326954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84433143-C-A

106326954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84433143-C-T

106327020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84433184-T-G

http://identifiers.org/hco/12/GRCh38#106327068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84433217-C-A

106327625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84433422-C-T

106327688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84433484-C-G

106328801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84434645-G-A

106328851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84434687-C-G

106328851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84434687-C-T

106329404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436069-C-T

106329416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436081-A-G

106329465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436110-A-G

106329467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436112-G-A

106329527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436172-T-A

106329561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436206-G-A

106329572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436217-A-G

http://identifiers.org/hco/12/GRCh38#106329620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436272-C-A

106329620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436272-C-T

http://identifiers.org/hco/12/GRCh38#106329622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436274-C-A

106329622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436274-C-G

http://identifiers.org/hco/12/GRCh38#106329624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436276-A-C

106329624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436276-A-G

106329638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436290-T-G

http://identifiers.org/hco/12/GRCh38#106329668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436320-C-A

106329668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436320-C-T

106329713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436364-A-G

http://identifiers.org/hco/12/GRCh38#106329734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436385-C-A

106329734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436385-C-T

106329882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436519-C-T

106329944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436568-G-A

106329993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436608-T-A

106330045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436696-T-C

106330048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436699-C-T

106330162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84436814-C-G

http://identifiers.org/hco/12/GRCh38#106330209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84436862-C-A

106330378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437013-C-G

106330378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437013-C-T

106330393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437019-G-T

106330397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437023-A-G

106330403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437029-G-A

106331043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437413-A-G

106331082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437418-G-A

106331218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437543-C-T

106331219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437544-T-C

106331238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437563-A-G

106331497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437968-G-A

http://identifiers.org/hco/12/GRCh38#106331509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84437981-C-A

106331509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437981-C-G

106331509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84437981-C-T

106331713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84438197-G-A

106331924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84438379-C-T

106332058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84438500-A-G

106334443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439522-C-T

106334562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439641-A-G

106334588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439667-T-G

106334593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439672-C-T

106334964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439727-T-G

106334983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439746-C-T

106335071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439813-T-C

106335148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439890-A-G

106335274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84439955-A-G

106335323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440007-T-C

106335422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440153-T-C

106335547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440271-G-T

106335677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: missense variant
orthologous variants: 84440409-G-A

106335735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: missense variant
orthologous variants: 84440461-C-T

106335745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: synonymous variant
orthologous variants: 84440471-A-T

106335761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: missense variant
orthologous variants: 84440487-T-G

http://identifiers.org/hco/12/GRCh38#106335859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84440584-A-C

106335941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440663-A-G

106335957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440679-A-G

106335988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440710-T-G

http://identifiers.org/hco/12/GRCh38#106336068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84440786-A-C

106336247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440965-G-A

106336247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84440965-G-T

http://identifiers.org/hco/12/GRCh38#106336281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84441014-A-C

106336282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441015-A-G

106336319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441051-G-T

106336454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441184-A-G

106336839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441309-C-T

106336932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441359-A-G

106337009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441420-C-G

106337051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441452-C-G

106337054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441455-A-G

106337072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441471-G-C

106337102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441490-A-G

106337191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441580-G-A

106337359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441720-C-T

http://identifiers.org/hco/12/GRCh38#106337367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84441728-A-C

106337401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441774-G-C

106337411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441783-C-T

106337426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441815-A-G

106337454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441844-T-C

106337537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84441928-T-C

106337612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84442013-A-G

106337660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84442057-C-T

106337690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84442085-T-G

106339762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84443122-G-T

106340065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84443410-C-T

http://identifiers.org/hco/12/GRCh38#106340249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84443583-C-A

106340249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84443583-C-G

106340249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84443583-C-T

106340401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84443726-A-G

106340697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444194-T-C

http://identifiers.org/hco/12/GRCh38#106340756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84444252-C-A

106340758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444254-G-A

106340758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444254-G-T

106340781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444283-T-A

106340799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444303-G-T

106340909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 84444412-T-C

http://identifiers.org/hco/12/GRCh38#106340946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84444449-A-C

http://identifiers.org/hco/12/GRCh38#106341048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84444556-C-A

106341069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444579-T-A

http://identifiers.org/hco/12/GRCh38#106341070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84444580-C-A

106341070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84444580-C-T

http://identifiers.org/hco/12/GRCh38#106341071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84444581-A-C

http://identifiers.org/hco/12/GRCh38#106341305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84445349-C-A

106341305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445349-C-G

106341305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445349-C-T

http://identifiers.org/hco/12/GRCh38#106341401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84445456-C-A

106341839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445786-T-C

106341867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445811-T-C

106341937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445875-C-T

106342020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445946-G-A

106342044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84445970-G-A

106342177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446108-G-A

106342224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446155-C-G

106342248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446179-C-T

106342376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446324-A-G

106342414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446353-T-C

106342910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446705-G-A

106342923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446719-G-A

106343031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446828-A-G

106343043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446840-G-A

106343189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84446972-A-T

106343370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84447138-T-C

106343430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84447189-G-A

http://identifiers.org/hco/12/GRCh38#106343544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84447290-C-A

http://identifiers.org/hco/12/GRCh38#106344446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84447833-A-C

106344624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84447990-A-G

106344624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84447990-A-T

106345319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84448479-G-A

106345607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84448762-A-G

106345753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84448886-G-A

106346027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84449129-T-G

106346067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: intron variant
orthologous variants: 84449169-G-C

106346549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3 prime UTR variant
orthologous variants: 84449596-C-G

106346549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3 prime UTR variant
orthologous variants: 84449596-C-T

http://identifiers.org/hco/12/GRCh38#106346648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84449683-A-C

106346648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3 prime UTR variant
orthologous variants: 84449683-A-G

106346682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28627
most severe consequence: 3 prime UTR variant
orthologous variants: 84449704-G-A