99828974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57420001-A-G

99829089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57419848-G-A

99829414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57419570-G-A

99829414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57419570-G-T

http://identifiers.org/hco/3/GRCh38#99829449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57419541-C-A

99829794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57419198-G-A

99829914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57419086-C-T

http://identifiers.org/hco/3/GRCh38#99829937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57419062-C-A

http://identifiers.org/hco/3/GRCh38#99830103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57418897-C-A

99830103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418897-C-T

99830175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418835-A-G

http://identifiers.org/hco/3/GRCh38#99830182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57418828-A-C

http://identifiers.org/hco/3/GRCh38#99830216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57418809-A-C

99830338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418661-G-T

99830342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418657-T-A

99830342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418657-T-C

http://identifiers.org/hco/3/GRCh38#99830683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57418298-C-A

99830683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57418298-C-G

99831344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414993-C-G

99831641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414765-G-T

99831840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414600-A-G

99831912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414528-C-T

99831913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414527-T-C

99832158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57414249-C-T

99833056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57413959-G-T

99833224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57413791-G-A

99833224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57413791-G-C

99833394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57413632-T-G

http://identifiers.org/hco/3/GRCh38#99833587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57406330-A-C

99833616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57406301-A-T

99833725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57406186-C-T

99833760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57406159-C-T

http://identifiers.org/hco/3/GRCh38#99833928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57406007-A-C

99834061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57405876-G-A

99834067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57405869-T-A

99834234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57405706-C-G

99834961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57404314-C-T

99835110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57404159-T-G

99835130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57404143-C-T

99835267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57404003-A-G

99835306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57403970-G-C

http://identifiers.org/hco/3/GRCh38#99835533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57403819-C-A

99835725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57403659-G-C

99836065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57403327-G-T

99836561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402877-C-G

99836575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402865-C-G

99836575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402865-C-T

http://identifiers.org/hco/3/GRCh38#99836634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57402806-A-C

http://identifiers.org/hco/3/GRCh38#99837222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57402216-C-A

99837377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402082-G-A

99837432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402010-G-A

99837440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57402002-A-G

99837464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57401990-T-C

99837539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57401927-T-G

99837728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57401773-G-T

99837794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57401703-A-G

99838416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57401124-T-G

99838852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57400733-C-T

99838885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57400688-C-G

http://identifiers.org/hco/3/GRCh38#99839135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57400413-C-A

99839135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57400413-C-T

99840944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57399323-A-G

99841155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57399120-G-A

99841155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57399120-G-T

99842759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57398632-A-G

99843050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57398383-A-G

99843265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57398206-G-C

99845340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57395663-A-G

99845489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57395434-C-T

99846052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57394904-G-A

99846432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57394582-G-A

99846439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57394575-T-C

99846745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57394264-G-T

99846841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57394181-T-C

http://identifiers.org/hco/3/GRCh38#99847115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57393893-C-A

99847192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57393819-G-T

99847646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57393413-G-A

99848108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57392979-T-G

99848374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57392707-T-A

99848754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57392327-G-A

99849321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57391760-G-A

99849321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57391760-G-C

99849833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57391248-T-C

99850399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57390682-G-A

99850914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57390167-G-A

99851035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57390046-T-G

99851039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57390042-A-G

99851083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57389998-A-G

99851150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57389938-T-C

http://identifiers.org/hco/3/GRCh38#99851320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57389759-C-A

99851562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57389572-G-A

99851768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57389354-T-C

99852204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57388241-G-A

99853119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386771-G-A

99853291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386659-G-A

99853501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386491-T-C

99853593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386430-A-G

99853677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386372-G-C

99853703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386349-T-C

99854844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57386286-G-A

99856190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57385784-C-G

99856473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57385516-C-T

http://identifiers.org/hco/3/GRCh38#99856630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57385373-A-C

99859671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57384373-C-G

99859671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57384373-C-T

99859908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57384176-C-T

99860662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57383541-T-A

99860682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57383527-G-A

99861344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57382687-G-A

99861642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57382468-A-G

99863045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57381931-C-T

99864143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57381071-T-C

99864161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57381054-C-T

99864164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57381051-C-G

99864205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57381026-C-T

99864585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57380710-C-G

99864980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57380152-G-A

99865556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57379617-C-T

99865696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57379476-T-C

http://identifiers.org/hco/3/GRCh38#99865770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57379419-A-C

99865867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57379330-T-C

99866399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57378734-T-G

99866849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57378294-T-C

99866901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57378245-C-G

99866901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57378245-C-T

99867134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57378041-A-G

99868111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57377209-T-C

99868169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57377152-T-C

99868221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57377095-T-C

99868453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57376877-T-A

http://identifiers.org/hco/3/GRCh38#99868663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57376662-C-A

99869042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57376351-C-G

99869189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57376251-T-C

99869605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57375747-A-G

99869697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57375642-T-A

99869697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57375642-T-C

99869929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57375418-A-G

99870303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57375129-G-A

99870904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57374330-G-C

99871214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57374066-A-T

99871323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57373962-C-G

99871958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57373439-C-T

99872412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57373013-T-C

99872658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372817-G-A

http://identifiers.org/hco/3/GRCh38#99872665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57372810-A-C

99872665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372810-A-T

99872706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372769-T-C

99872927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372556-T-C

99873080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372409-G-A

99873361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372208-C-T

99873408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372162-T-C

99873451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57372137-T-A

99875243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57370474-T-C

99875765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369966-G-T

http://identifiers.org/hco/3/GRCh38#99875967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57369803-C-A

99875967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369803-C-T

http://identifiers.org/hco/3/GRCh38#99876049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57369723-C-A

99876049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369723-C-G

99876049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369723-C-T

99876075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369697-A-G

99876318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369489-G-A

99876318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369489-G-C

99876318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369489-G-T

99876414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57369410-C-T

99877138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57368701-C-T

99877331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57368505-A-G

99877389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57368477-G-A

99877478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57368375-A-G

99877693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57368165-A-T

http://identifiers.org/hco/3/GRCh38#99878214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57367670-C-A

99878825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57367066-T-G

99878880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57367013-C-G

99878912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57366981-T-G

99881110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57365158-T-C

99881225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57365051-T-C

99881441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57364854-C-T

99881853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57364755-C-T

99881892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57364715-T-A

99890263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57362460-C-T

99890381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57362349-G-A

99890455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57362279-T-C

99890464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57362268-T-G

99890580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57362095-T-A

99890685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361995-T-C

99890942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361767-C-T

99891071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361640-C-T

99891143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361566-T-C

99891151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361558-C-T

99891495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361264-G-A

99891513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57361246-T-G

99891903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360939-A-G

99892115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360862-A-G

99892216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360764-T-G

99892442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360538-A-G

99892474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360425-C-T

99892504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360354-T-G

99892555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360304-C-G

99892656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360219-A-G

99892760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57360164-T-A

99892935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57359994-C-T

99893618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57359629-G-A

99894192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57359059-G-C

99894246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57359002-G-T

99894397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358869-C-T

99894422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358844-C-T

99894595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358650-G-A

99894669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358567-C-T

99894679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358557-A-T

99894753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358481-C-T

99894846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358390-G-A

99894869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358367-C-T

http://identifiers.org/hco/3/GRCh38#99894937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57358304-A-C

99894937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57358304-A-G

http://identifiers.org/hco/3/GRCh38#99895399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57357863-A-C

99895399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57357863-A-G

99895399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57357863-A-T

99895407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57357855-C-T

99895741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57357522-T-C

http://identifiers.org/hco/3/GRCh38#99895794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57357486-C-A

99898850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57354693-A-G

99898941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57354331-A-G

99898974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57354300-A-G

99899378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353925-T-A

99899700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353605-G-A

99899743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353574-C-T

99899783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353533-C-T

99899784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353532-A-G

99900737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353418-C-T

99900740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353416-G-A

99900913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353280-T-C

99901129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57353069-T-C

99901217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57352976-G-A

99902212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57351897-T-C

http://identifiers.org/hco/3/GRCh38#99902340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57351772-A-C

99902340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57351772-A-T

99902507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57351616-G-A

99902507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57351616-G-T

99903590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350818-G-A

99903760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350678-G-A

99903760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350678-G-T

99904009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350389-C-T

99904117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350288-A-G

99904357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57350049-A-G

99904441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349936-C-G

http://identifiers.org/hco/3/GRCh38#99904552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57349847-C-A

99904609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349795-T-A

99904722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349701-T-G

99905127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349323-C-G

99905144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349305-T-G

99905487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57349036-A-G

99908330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347786-A-G

99908330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347786-A-T

99908343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347773-T-A

99908501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347618-A-G

99908694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347435-G-T

99908708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347421-A-G

99908730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57347403-G-A

99909014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346993-T-A

99909264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346732-G-A

99909267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346729-G-A

99909282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346714-A-G

99909577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346424-G-C

99909637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346355-T-C

99909677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346295-A-G

99909692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346267-A-G

99909692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346267-A-T

99909703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346230-A-G

99909766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346169-G-T

99909821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346113-G-A

99909900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57346034-A-G

99909973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57345961-C-T

99910207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57345732-A-G

http://identifiers.org/hco/3/GRCh38#99910779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57345447-A-C

99910900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57345340-G-C

99911025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57345216-A-G

99911301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57344949-G-C

http://identifiers.org/hco/3/GRCh38#99914115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57342631-A-C

99914233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57342512-T-C

http://identifiers.org/hco/3/GRCh38#99914271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57342472-A-C

99915345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57341228-C-T

http://identifiers.org/hco/3/GRCh38#99915559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57341020-C-A

99915627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340952-G-A

http://identifiers.org/hco/3/GRCh38#99915691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57340887-C-A

99915691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340887-C-G

99916074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340511-C-T

99916405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340176-C-T

99916483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340115-C-T

99916523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340075-T-C

99916543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57340055-T-C

99916664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57339566-T-C

99916926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57339332-T-C

99916938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57339320-G-A

http://identifiers.org/hco/3/GRCh38#99916993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57339265-C-A

http://identifiers.org/hco/3/GRCh38#99917030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57339229-A-C

99917076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57339183-C-G

http://identifiers.org/hco/3/GRCh38#99917385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57338865-A-C

99917776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338476-A-G

99918361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338366-C-G

99918375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338351-C-G

99918557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338190-C-G

99918592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338155-G-A

99918633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57338130-T-C

99918985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57337794-A-G

99919001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57337778-T-C

99919072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57337712-A-T

99919104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57337680-G-C

http://identifiers.org/hco/3/GRCh38#99919579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57337249-A-C

99919579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57337249-A-T

http://identifiers.org/hco/3/GRCh38#99919817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57337022-A-C

99919882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336957-G-C

99920279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336595-T-G

99920403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336459-C-G

99920644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336220-C-T

http://identifiers.org/hco/3/GRCh38#99920666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57336198-C-A

99920666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336198-C-T

http://identifiers.org/hco/3/GRCh38#99920681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57336183-A-C

99920701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336163-T-A

http://identifiers.org/hco/3/GRCh38#99920839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57336024-A-C

99920839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57336024-A-G

http://identifiers.org/hco/3/GRCh38#99920929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57335959-A-C

99921307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335606-C-T

99921374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335561-A-G

99921486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335454-G-C

99921506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335434-A-G

99921639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335320-C-T

99921873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335126-C-T

http://identifiers.org/hco/3/GRCh38#99921952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57335049-C-A

99921952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57335049-C-T

99922055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57334954-C-G

99922552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57334479-A-T

99923773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57334199-G-C

99923800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57334172-C-G

99924052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333971-C-G

99924079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333944-T-C

99924085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333938-C-T

99924109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333916-G-T

99924215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333821-C-G

99924366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333669-T-C

99924468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333560-T-A

99926371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57333121-T-C

http://identifiers.org/hco/3/GRCh38#99926686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57332638-A-C

99926833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57332330-T-C

99927050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57331926-C-T

99927131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57331852-G-T

http://identifiers.org/hco/3/GRCh38#99927202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57330015-C-A

99927202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57330015-C-T

99927908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329663-T-C

99927924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329648-C-G

99927924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329648-C-T

99928257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329415-C-T

99928274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329398-G-A

99928660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329128-A-G

99928760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57329063-A-G

99929723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57328233-T-A

99929751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57328206-A-T

99929780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57328178-G-T

99929878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57328061-A-G

99929956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327983-A-G

99929965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327974-T-G

99929995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327944-T-G

http://identifiers.org/hco/3/GRCh38#99930038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57327901-A-C

99930038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327901-A-G

99930104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327834-T-G

99930419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327534-T-C

99930636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327348-A-T

99930669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327315-G-A

99930669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327315-G-T

99930745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327239-G-A

99930793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57327191-G-A

99930872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 57327112-C-T

99930949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57327044-A-G

http://identifiers.org/hco/3/GRCh38#99931090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57326903-C-A

99931090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57326903-C-G

99931090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57326903-C-T

http://identifiers.org/hco/3/GRCh38#99931131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57326863-C-A

http://identifiers.org/hco/3/GRCh38#99931546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57326476-A-C

http://identifiers.org/hco/3/GRCh38#99931606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57326415-A-C

99931793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57326269-G-A

99931831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57326235-T-C

99932487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57325543-T-A

99932513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57325503-A-G

99933830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57324399-T-C

99933889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57324341-C-T

99933909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57324321-A-G

99934273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57323966-G-A

99934881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57323435-A-G

99935244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57323089-G-A

99935785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57322604-C-G

99935920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57322465-G-A

99936071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57322337-A-G

99936206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57322205-G-A

http://identifiers.org/hco/3/GRCh38#99937676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57321413-A-C

99937714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321368-A-T

99937727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321355-G-A

99937739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321349-G-T

99937760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321328-G-T

99937811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321277-T-G

99938115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57321043-G-T

99938924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57320328-A-G

99938967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57320286-T-C

99944606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57318018-A-G

99945544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57317233-G-A

99945857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316917-T-A

99945857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316917-T-C

99945911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316866-C-T

99946185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316590-A-T

http://identifiers.org/hco/3/GRCh38#99949354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57316526-A-C

99949354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316526-A-G

99949559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316366-A-G

99949559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316366-A-T

99949680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316241-T-A

99949876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57316042-A-T

99949944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315912-A-G

99950464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315431-C-T

99950552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315335-T-C

99950560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315327-A-G

99950563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315324-G-A

99950564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57315323-G-T

http://identifiers.org/hco/3/GRCh38#99950983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57314976-A-C

99951768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57313680-A-G

http://identifiers.org/hco/3/GRCh38#99951898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57313066-A-C

99951898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57313066-A-G

99952263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312711-A-G

99952360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312607-T-C

99952386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312582-G-A

99952577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312389-C-T

http://identifiers.org/hco/3/GRCh38#99952689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57312254-C-A

99952803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312133-G-A

99952803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312133-G-C

99952860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57312077-A-G

99953270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57311719-C-G

http://identifiers.org/hco/3/GRCh38#99953426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57311600-A-C

http://identifiers.org/hco/3/GRCh38#99956179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57308597-C-A

99956179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57308597-C-T

http://identifiers.org/hco/3/GRCh38#99956914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57308334-A-C

99956914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57308334-A-G

99957162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57308116-G-A

99957195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57308081-C-G

99957208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57308068-G-C

99957290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307970-C-T

99957599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307678-C-T

99957627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307652-C-T

99957725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307545-G-T

99958445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307338-T-C

99958543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307270-G-A

99958543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307270-G-T

99958697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57307134-T-C

99958886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57306951-G-A

99959055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57306154-G-A

99959055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57306154-G-C

99959841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57305779-A-G

99959881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57305738-G-A

99959986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57305643-G-T

99960409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57305199-G-C

99960414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57305194-T-C

99960884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304756-G-A

99961197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304454-A-T

99961339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304315-T-A

99961339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304315-T-C

99961417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304240-A-G

99961516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57304137-C-T

99961759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303940-A-G

99962029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303706-G-A

99962036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303699-T-A

http://identifiers.org/hco/3/GRCh38#99962127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57303629-C-A

99962253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303514-A-T

99962333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303434-C-T

99962387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303382-A-G

99962612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57303194-A-T

99962923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302889-G-A

99962971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302855-G-A

99963996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302552-C-G

99964202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302348-C-T

http://identifiers.org/hco/3/GRCh38#99964263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57302309-C-A

99964285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302303-A-G

99964409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302259-G-A

99964409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302259-G-T

99964425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302243-G-A

99964425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302243-G-T

99964546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57302192-T-C

99964777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57301973-G-T

99965322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57301510-T-C

99965326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57301506-C-T

http://identifiers.org/hco/3/GRCh38#99966217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57301188-C-A

99966217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57301188-C-G

99966274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57301132-T-G

99967553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57298737-A-G

99967643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57298651-A-G

99968395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57297928-A-G

99969007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57297477-C-G

99969778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57296321-G-A

99969812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57296288-A-G

99969992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57296188-T-C

99970061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57296082-T-C

99970197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57295954-A-G

99971943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294899-T-C

99972088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294759-A-G

99972091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294756-T-C

99972340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294539-C-T

99972581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294304-G-C

99972581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294304-G-T

99972661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57294224-T-C

99973232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293721-A-G

99973232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293721-A-T

99973353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293656-T-C

99973720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293305-A-G

99973930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293124-T-C

99973930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57293124-T-G

99974074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57292982-A-G

http://identifiers.org/hco/3/GRCh38#99974139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57292921-C-A

99974340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57292724-T-C

99974876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57292498-G-A

99974981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57292382-A-G

http://identifiers.org/hco/3/GRCh38#99975074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57292290-C-A

99975312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57292112-A-G

http://identifiers.org/hco/3/GRCh38#99976382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57291476-A-C

99976536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57291326-T-C

99976606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57291256-A-G

99976615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57291247-A-G

99976631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57291229-A-G

99976814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57291099-A-G

99976921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57290994-A-G

99976982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57290933-A-G

99977208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57289145-G-A

99977217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57289136-G-A

99977217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57289136-G-C

99977368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57289003-T-C

99977375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57288996-A-T

99977424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57288954-A-G

99977427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57288951-C-G

99977818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57288587-C-T

99978194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57288211-C-T

99979578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57287530-A-G

99979890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57287221-G-A

99979935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57287183-T-C

99979973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57287143-G-A

99980013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57287104-T-C

http://identifiers.org/hco/3/GRCh38#99980232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57286894-A-C

99980261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286880-C-T

99980407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286758-A-G

99980413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286752-T-C

http://identifiers.org/hco/3/GRCh38#99980569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57286598-A-C

99980760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286413-A-G

http://identifiers.org/hco/3/GRCh38#99980880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57286309-C-A

99981001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286212-G-C

99981161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286076-G-A

99981189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57286048-C-T

99981267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285987-T-C

99981291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285957-T-C

99981740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285820-T-A

99981785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285783-G-A

99981816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285752-T-G

99982694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285025-A-G

99982700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57285019-G-A

99982743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284976-A-G

99982843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284880-A-G

99982942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284785-A-G

99982956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284771-G-A

99983107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284639-G-A

99983107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284639-G-C

99983855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284392-T-C

99984032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57284222-A-G

99984721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57283558-T-C

99984912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57283209-G-A

99984983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57283156-G-A

99985163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57283003-A-T

99985254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57282910-C-T

99985512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57282765-A-G

99987569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57281366-G-A

99987569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57281366-G-C

99987880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57281082-T-C

99987958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57280997-A-G

99988029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57280924-C-T

99988539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57280746-A-G

http://identifiers.org/hco/3/GRCh38#99988724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57280540-A-C

http://identifiers.org/hco/3/GRCh38#99988728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57280536-C-A

99988859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57280434-A-G

99998967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277622-A-G

http://identifiers.org/hco/3/GRCh38#99998996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57277591-C-A

99998996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277591-C-G

99999194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277424-C-G

99999290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277024-T-C

99999301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277013-T-C

99999301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57277013-T-G

99999734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276600-T-C

99999927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276423-G-A

99999980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276367-T-C

99999980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276367-T-G

100000010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276354-A-G

100000016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276348-C-T

100000131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276243-C-T

100000266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276130-G-A

100000424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57276006-C-T

100000808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57275738-T-C

100001307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57275293-T-C

100001811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57274662-T-A

100001811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57274662-T-G

100002140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57274349-G-C

100002260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57274223-C-G

100002724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57274002-G-T

100002903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57273781-A-G

100002972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57273716-C-G

100003145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57273547-C-T

100003270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57273463-C-T

100003413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57273327-T-C

100003981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57272752-G-A

100004029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57272673-A-G

100004087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57272534-G-C

100004087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57272534-G-T

100004178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57272463-T-C

100004495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271979-A-G

100005610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271743-G-C

100005839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271552-G-A

100005952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271426-T-C

100005986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271393-T-A

100006160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57271251-T-C

100006903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57270506-G-A

100006903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57270506-G-T

100007505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57269964-T-C

100007546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57269748-G-T

100007611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57269684-G-A

100007617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57269678-A-G

http://identifiers.org/hco/3/GRCh38#100008180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57267226-A-C

100008206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57267200-A-G

100008320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57267090-G-A

100008320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57267090-G-C

100008354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57267056-A-G

100008689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266727-A-G

100008853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266584-A-T

100008901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266534-G-A

100008933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266502-A-G

100009169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266275-T-C

100009406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57266045-T-G

http://identifiers.org/hco/3/GRCh38#100009647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57265801-C-A

100009647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57265801-C-G

100009685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57265763-A-G

100009698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57265750-A-G

100010473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57265041-T-A

100010973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264884-C-G

100011106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264759-T-C

100011114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264752-G-A

100011191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264681-A-G

100011293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264609-G-A

100011293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264609-G-C

100011342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264545-A-G

100011361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264529-C-T

100011424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57264467-A-G

http://identifiers.org/hco/3/GRCh38#100011956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57263599-A-C

100012179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57263383-A-G

100012475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57263113-A-G

100012494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57263094-G-A

http://identifiers.org/hco/3/GRCh38#100012549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57263052-A-C

100012604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57263007-C-T

100012611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57262999-G-A

100012622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57262984-T-C

100012661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57262937-C-T

100017030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261907-T-C

100017078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261858-T-C

100017147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261782-A-T

100017151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261778-A-G

100017234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261700-T-C

100017333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261629-A-G

100021118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261312-T-A

100021362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57261052-T-C

100021540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57260886-C-T

http://identifiers.org/hco/3/GRCh38#100021551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57260861-C-A

100021592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57260809-A-T

100021698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57260717-A-G

100021872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57260615-C-G

100021958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57260083-T-A

http://identifiers.org/hco/3/GRCh38#100022008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57260032-C-A

100022161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259903-G-A

100022570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259529-T-C

100022611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259502-T-G

100022741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259392-T-G

100022913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259223-T-C

http://identifiers.org/hco/3/GRCh38#100022964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57259174-A-C

100022965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57259173-A-G

http://identifiers.org/hco/3/GRCh38#100023199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57258953-C-A

100023223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57258941-T-A

http://identifiers.org/hco/3/GRCh38#100023422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57258742-C-A

100023422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57258742-C-G

100024201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57258006-A-T

100024405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257799-C-T

100024525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257549-T-C

100024855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257233-A-G

http://identifiers.org/hco/3/GRCh38#100024891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57257197-A-C

100024891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257197-A-G

100024891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257197-A-T

100024954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57257152-A-G

100025137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255998-T-G

100025269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255860-G-T

100025309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255839-A-G

100025323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255825-G-T

100026234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255677-C-T

100026270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255641-A-G

100026385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255527-A-G

100026385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255527-A-T

http://identifiers.org/hco/3/GRCh38#100026591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57255342-A-C

100026591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255342-A-G

100026846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255089-A-G

100026903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57255033-C-G

100027048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254890-G-A

100027103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254829-G-A

100027133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254795-A-G

100027235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254692-A-G

100027480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254458-T-C

100027554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57254388-C-T

100027789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

100028665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57253117-T-C

http://identifiers.org/hco/3/GRCh38#100028809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57252949-A-C

100028905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252797-A-G

100028953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252747-T-C

100029297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252581-G-T

100029432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252460-C-T

100029540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252372-C-T

100029598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252338-C-G

100029610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252321-A-G

100029824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252144-T-G

100029851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252120-A-G

100029914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252039-G-C

100029914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252039-G-T

http://identifiers.org/hco/3/GRCh38#100029937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57252016-C-A

100029937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252016-C-T

100029951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57252002-G-C

100030105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57251851-G-A

100030132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57251813-A-G

100030199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57251750-A-G

100030318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57251630-C-T

100030625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57251369-A-G

100031285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57250386-G-T

100031639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57250054-C-T

100031641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57250052-T-G

100031794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57249919-C-T

100031822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57249890-A-G

100031976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57249758-C-T

100032028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57249721-A-G

100032219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57249521-G-T

100032833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57248881-T-A

100032833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57248881-T-C

http://identifiers.org/hco/3/GRCh38#100033000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57248500-C-A

100033155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57248323-T-C

100033163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57248315-G-A

http://identifiers.org/hco/3/GRCh38#100033199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57248280-A-C

100033199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57248280-A-G

100033715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247791-T-A

100033716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247790-A-T

100033788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247723-C-T

100033894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247630-A-G

100034315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247280-C-T

100034340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57247255-T-C

http://identifiers.org/hco/3/GRCh38#100034484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57247112-A-C

http://identifiers.org/hco/3/GRCh38#100035092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57246528-A-C

100035095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57246525-G-T

100035800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57245701-C-T

100037253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57244539-A-G

100037334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57244459-A-G

100039617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57242953-G-A

100039938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242887-A-G

100040137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242762-T-C

100040181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242718-G-A

http://identifiers.org/hco/3/GRCh38#100040371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57242551-C-A

100040371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242551-C-G

100040371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242551-C-T

100040397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242524-A-G

100040421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242500-G-T

100040495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242423-G-T

100040496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242422-C-T

100040501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242417-T-G

http://identifiers.org/hco/3/GRCh38#100040524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57242392-C-A

100040524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242392-C-T

100040544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242372-T-C

100040600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242308-T-C

100040604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242304-A-G

http://identifiers.org/hco/3/GRCh38#100040609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57242299-C-A

100040730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242193-T-C

100040809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242114-T-C

100040839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242085-A-G

100040855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57242067-G-T

100041026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57241902-G-A

http://identifiers.org/hco/3/GRCh38#100041157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57241772-C-A

100041334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57241594-G-A

http://identifiers.org/hco/3/GRCh38#100041465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57241454-C-A

100041819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57241082-G-T

100041965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240965-T-C

100041965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240965-T-G

100042097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240811-T-A

100042448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240452-T-C

100042569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240357-A-T

100042610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57240316-T-C

100043044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57239892-C-G

100043106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57239835-T-C

100043365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57239584-A-G

http://identifiers.org/hco/3/GRCh38#100044195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57238333-C-A

100044195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57238333-C-T

100045147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57237382-G-A

100045176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57237354-A-G

100045191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57237300-C-T

100045218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57237273-G-T

100045484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236974-T-C

100045899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236584-C-T

100045923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236560-G-A

100045923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236560-G-T

100046155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236319-C-T

100046449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236044-A-T

100046474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236023-A-G

100046474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57236023-A-T

100046608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57235901-G-A

100046643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57235877-G-C

100046971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234837-G-T

100047075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234736-A-G

100047248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234548-G-A

100047429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234281-C-T

100047552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234137-C-T

100047574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57234116-A-G

100048622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57233167-G-A

100048626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57233163-G-A

100048824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57232983-A-G

100049149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57232259-T-C

100049218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57232198-A-G

100049407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57232021-C-T

http://identifiers.org/hco/3/GRCh38#100049411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57232017-A-C

http://identifiers.org/hco/3/GRCh38#100049416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57232012-A-C

100050409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57231208-A-G

100050480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57231130-T-C

100050480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57231130-T-G

100050534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57231079-T-C

100050622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57230961-C-T

100050900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57230716-C-T

100051044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57230570-T-A

100051290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57230173-A-G

100051298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57230165-G-A

100051302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57230161-G-A

100051892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57230025-T-C

100052041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57229914-T-G

100052172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57229840-A-G

100052217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57229795-G-A

100052219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57229793-A-G

100052671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57229248-T-G

100053082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57228495-A-G

100053707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57227885-G-A

100053797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57227798-A-G

100054231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57227379-C-T

100054459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57227164-A-G

100054645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57227062-A-G

100054982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226741-C-T

100054986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226737-T-G

100055110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226620-T-G

100055292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226439-C-T

100055375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226360-T-C

100055375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57226360-T-G

100057598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225774-T-A

100057657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225715-C-T

100057905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225478-T-C

100058001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225389-A-G

100058107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225302-G-T

100058115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57225294-C-G

100058561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57224925-C-G

100058769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57224647-T-C

100059304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57224122-T-A

http://identifiers.org/hco/3/GRCh38#100059568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57223897-A-C

100059684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223809-A-G

100059808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223704-G-A

100059893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223607-G-A

100059978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223523-T-C

100059991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223510-C-G

100059991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57223510-C-T

100063664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57222785-A-T

100063970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57222515-C-T

100064399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57222075-T-C

100064555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221926-A-G

100064735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221741-T-A

http://identifiers.org/hco/3/GRCh38#100064759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57221715-C-A

100064780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221694-G-T

100064810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221663-T-A

100065004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221526-C-G

100065215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57221252-G-A

100066262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57220930-A-G

100066463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57220745-G-A

100066907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57220617-C-T

100067075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57220470-A-G

100068883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57219246-T-G

100068962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57219166-G-A

100068962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57219166-G-C

100069065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57219080-T-C

100069153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218992-A-G

100069361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218759-G-T

100069419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218720-C-G

100069533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218549-C-G

100069533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218549-C-T

100069810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218212-G-T

100069877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218153-C-T

100069987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218041-T-A

100069987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57218041-T-C

http://identifiers.org/hco/3/GRCh38#100070163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57217867-C-A

100070163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217867-C-G

100070216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217815-C-T

100070227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217804-A-G

100070608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217454-T-A

100070940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217245-C-T

100071121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217132-A-T

100071189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217071-A-G

100071210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57217050-G-T

http://identifiers.org/hco/3/GRCh38#100071306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57216967-A-C

100071357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216916-G-A

100071455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216828-C-G

100071455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216828-C-T

100071491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216792-C-T

100071518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216765-G-C

100071535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216750-A-G

100072001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216245-G-A

100072035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57216213-G-A

100072346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57215967-G-A

100072648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57215727-A-G

100072648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57215727-A-T

100073575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57214198-G-A

100073963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57213840-C-T

100074477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, undefined
orthologous variants: 57213333-G-A

100075667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210970-T-C

http://identifiers.org/hco/3/GRCh38#100075680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57210951-C-A

http://identifiers.org/hco/3/GRCh38#100075693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57210937-C-A

100075785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210860-G-A

100075887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210760-G-T

http://identifiers.org/hco/3/GRCh38#100075947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57210706-A-C

100076085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210561-T-G

100076090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210556-A-G

100076116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210530-T-G

100076284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210377-C-G

100076284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210377-C-T

100076293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210368-A-G

100076453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210247-G-C

100077002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57210128-C-T

100077215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57209917-C-G

100077278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57209884-A-G

100077286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57209876-A-G

100079081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57208760-G-A

http://identifiers.org/hco/3/GRCh38#100079264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57208546-C-A

100079805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57208035-T-C

100080602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57206281-T-C

100080622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57206261-A-T

100080957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205874-G-C

100081162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205664-A-G

100081364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205498-G-A

http://identifiers.org/hco/3/GRCh38#100081618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57205345-A-C

100081631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205333-G-A

100081797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205149-T-C

100081826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205093-G-A

100081908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57205020-T-A

100082244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57204692-G-C

100082583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57204369-G-A

http://identifiers.org/hco/3/GRCh38#100082607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57204345-A-C

100082663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57204291-C-T

100082697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57204257-T-C

100083212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57203747-C-G

100083246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57203713-C-T

100083247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57203712-T-C

100083385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57203564-C-T

http://identifiers.org/hco/3/GRCh38#100084069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57202623-C-A

100084171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57202524-G-A

100084213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57202482-T-A

100085034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57201091-G-A

100085078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57201070-T-C

100085086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57201062-A-G

100085203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57200949-C-T

100085338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57200451-T-C

100085613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57200188-A-G

100085738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57200071-A-T

100085753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57200056-C-T

100086196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199617-G-A

100086238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199561-T-C

100086435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199371-G-A

100086435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199371-G-C

100086435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199371-G-T

100086454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199352-T-G

100086476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199338-A-G

100086594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199273-A-G

100086653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199212-A-T

100086672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199193-T-C

100086679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57199186-G-T

100086994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198916-A-G

100086994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198916-A-T

100087023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198888-T-C

100087190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198739-G-C

100087229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198703-G-A

100087303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198647-G-A

100087421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57198542-T-C

http://identifiers.org/hco/3/GRCh38#100088321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57198141-A-C

100089192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57197198-G-A

100089219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57197171-T-G

100089383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196999-A-G

100089439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196934-G-A

100089601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196809-G-A

100089665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196753-T-C

100089679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196730-A-G

100089977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57196353-C-T

100090376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57195976-A-G

100090702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57195575-A-G

100091849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57194467-T-G

100092009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57194326-C-T

100092315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57193911-T-C

100092367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57193859-G-A

100092396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57193799-A-G

http://identifiers.org/hco/3/GRCh38#100092600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57193600-A-C

100092673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57193528-A-G

http://identifiers.org/hco/3/GRCh38#100092706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57193497-C-A

http://identifiers.org/hco/3/GRCh38#100092765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57193446-C-A

100098890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57192690-T-C

100099413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57192170-A-T

100100305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57191155-T-C

100100937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57190628-T-G

100101030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57190551-A-G

100101591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57190088-C-T

100102365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57190074-T-C

100102532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57189549-A-T

100102533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57189548-C-T

100102846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57189087-G-A

100103133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188729-C-G

100103211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188648-T-C

100103252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188612-C-G

100103323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188560-G-A

100103363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188520-T-C

100103419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188486-G-A

100103838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188236-T-C

100103928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188151-T-G

100104040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188034-A-T

100104044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188030-G-T

100104070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188007-G-A

100104071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57188006-G-A

100104146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187982-A-G

http://identifiers.org/hco/3/GRCh38#100104583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57187556-C-A

100104583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187556-C-T

100104657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187485-C-G

100104927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187401-G-A

100105216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187143-G-A

100105229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57187131-A-T

100106619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57185997-T-A

http://identifiers.org/hco/3/GRCh38#100106913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57185740-A-C

100106916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57185739-T-C

100106934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57185721-T-G

100107295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57185091-A-T

100107401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57184994-T-C

100107550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57184872-C-T

100107639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57184784-T-G

100107671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57184753-G-T

100107975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57184450-T-C

100108523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182974-C-T

100108744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182740-C-T

100108788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182702-G-A

100108807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182684-C-T

100109081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182385-G-T

100109205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182271-G-A

100109205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182271-G-T

100109211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57182265-T-A

100109257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57180676-A-G

100109508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57180413-A-G

100109511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57180410-A-T

100109560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57180367-G-A

100110472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57177331-A-G

100110874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57176843-T-C

100110874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57176843-T-G

100111233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57176492-A-G

100111360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57176367-G-C

100111627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57176121-A-G

100111912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57175786-A-G

100111993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57175722-C-T

100112362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57175351-G-A

http://identifiers.org/hco/3/GRCh38#100112382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57175331-C-A

100113218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57174624-C-G

100113363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57174481-A-T

100113398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57174445-T-C

100113811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57174060-A-T

100113876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57173999-T-C

http://identifiers.org/hco/3/GRCh38#100113979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57173890-C-A

100113979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57173890-C-T

100114075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57173801-T-C

http://identifiers.org/hco/3/GRCh38#100114110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57173766-C-A

100114235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57173645-A-T

http://identifiers.org/hco/3/GRCh38#100114239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57173641-C-A

100114250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57173630-A-G

http://identifiers.org/hco/3/GRCh38#100114365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57173515-C-A

100114365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57173515-C-T

100114433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24589
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57173446-A-G