20567380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57661701-C-G

20567406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57661734-A-G

20567406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57661734-A-T

20567441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57661766-C-T

20567527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57661846-G-C

20567527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57661846-G-T

http://identifiers.org/hco/13/GRCh38#20567633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57661908-A-C

20567633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57661908-A-G

20567640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57661916-G-A

20567723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57661984-T-A

20568175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57662484-C-G

20568363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57662609-T-C

20568369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57662615-C-G

20570914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57666087-G-T

20573511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57667435-T-C

20573639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57667540-G-A

20573916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57667797-T-G

http://identifiers.org/hco/13/GRCh38#20574293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57667932-C-A

20574293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57667932-C-T

20574526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668138-T-A

20574526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668138-T-C

20574539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668151-G-A

20574539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668151-G-C

20574595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668206-A-G

20574678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57668287-C-G

20582092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57671282-G-T

20582245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57671381-A-G

20582531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57671580-G-A

20582531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57671580-G-T

20582688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57671847-C-T

20582815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672078-G-C

20582815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672078-G-T

20582906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672209-T-C

20582932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672227-T-A

http://identifiers.org/hco/13/GRCh38#20583019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57672314-A-C

20583019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 57672314-A-G

20583052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672340-A-G

20583052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672340-A-T

http://identifiers.org/hco/13/GRCh38#20583077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57672363-C-A

20583077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672363-C-T

20583136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672399-G-T

20583167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57672429-G-T

20589705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674342-A-G

http://identifiers.org/hco/13/GRCh38#20589729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57674619-C-A

20589797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674670-T-C

http://identifiers.org/hco/13/GRCh38#20589815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57674688-C-A

20589846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57674719-A-G

20589851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57674724-T-C

http://identifiers.org/hco/13/GRCh38#20589912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57674760-C-A

20589912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674760-C-G

20589912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674760-C-T

20589933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674779-T-A

20589933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674779-T-C

20589938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674784-A-G

http://identifiers.org/hco/13/GRCh38#20589966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57674811-C-A

20589966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674811-C-T

20590146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57674971-G-A

20590324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675147-G-A

20590433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675280-A-G

20590572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675330-G-A

http://identifiers.org/hco/13/GRCh38#20590847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57675566-A-C

20590855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675573-A-G

http://identifiers.org/hco/13/GRCh38#20590856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57675574-A-C

20590856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675574-A-T

20590973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57675705-A-T

20590987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57675719-A-G

http://identifiers.org/hco/13/GRCh38#20591079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57675808-C-A

20591079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675808-C-T

20591152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675865-T-A

20591152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675865-T-C

20591253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675963-A-G

20591253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57675963-A-T

20591458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676174-A-G

http://identifiers.org/hco/13/GRCh38#20591500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57676216-A-C

20591576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676276-T-C

20591585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676285-T-C

20591594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676294-A-G

20591607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676312-T-G

http://identifiers.org/hco/13/GRCh38#20591767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57676447-A-C

20591830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57676622-G-T

20592218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677071-T-C

20592295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677128-G-A

20592295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677128-G-T

20592414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677242-T-C

20592414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677242-T-G

20592476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677298-A-G

20592476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677298-A-T

http://identifiers.org/hco/13/GRCh38#20592981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57677433-A-C

20592981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677433-A-G

20594964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57677558-G-A

20596111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678354-T-C

20596114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678357-A-G

20596124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678367-A-G

20596339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678579-G-A

20596545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678802-G-T

http://identifiers.org/hco/13/GRCh38#20596929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57679259-C-A

20596929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57679259-C-T

20597193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57680603-T-A

http://identifiers.org/hco/13/GRCh38#20598079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57681061-A-C

20598350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681343-A-G

http://identifiers.org/hco/13/GRCh38#20598352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57681345-C-A

20598352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681345-C-T

20598417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681412-T-C

20598417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681412-T-G

http://identifiers.org/hco/13/GRCh38#20598434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57681429-A-C

20598465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681459-G-C

20598524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681511-A-G

20598524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681511-A-T

20598595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681761-G-T

http://identifiers.org/hco/13/GRCh38#20598606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57681772-C-A

20598606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681772-C-T

20598611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681777-G-T

20598797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681948-G-A

20598797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681948-G-T

20598834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57681982-T-A

20599424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683003-T-C

20599424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683003-T-G

http://identifiers.org/hco/13/GRCh38#20599628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57683193-C-A

20599628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683193-C-G

http://identifiers.org/hco/13/GRCh38#20599715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57683290-A-C

20599715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683290-A-T

20599793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683369-C-T

20599915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683479-G-A

20599915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683479-G-C

http://identifiers.org/hco/13/GRCh38#20600239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57683680-C-A

20600675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57684024-A-G

20601385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57684727-A-G

20601387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57684729-T-A

20601387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57684729-T-C

http://identifiers.org/hco/13/GRCh38#20601578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57684869-A-C

20601578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57684869-A-G

http://identifiers.org/hco/13/GRCh38#20601687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57684980-C-A

20601708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57685001-T-G

20604433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57687849-G-A

20604433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57687849-G-C

20604568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57687986-T-A

20604584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57688003-A-G

20604638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57688052-A-G

20605055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57688148-A-G

http://identifiers.org/hco/13/GRCh38#20605570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57689312-C-A

20605914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57689697-C-T

20615704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692826-G-T

20615724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692846-A-G

20615724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692846-A-T

http://identifiers.org/hco/13/GRCh38#20615759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57692884-C-A

20615759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692884-C-T

http://identifiers.org/hco/13/GRCh38#20615768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57692893-C-A

20615768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692893-C-G

20615768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57692893-C-T

20615856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57692981-A-G

http://identifiers.org/hco/13/GRCh38#20625707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57710388-C-A

20625858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57710540-T-A

http://identifiers.org/hco/13/GRCh38#20625882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57710543-C-A

20625882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57710543-C-T

20625883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57710544-A-G

20625883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57710544-A-T

20626551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57710844-C-T

20627294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57711589-A-G

20627360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57711662-G-A

http://identifiers.org/hco/13/GRCh38#20629474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57712190-A-C

20629474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57712190-A-G

20629627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57712370-A-G

20629941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57712651-A-T

20630077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57712775-G-T

20630357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713037-A-G

20630397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713074-A-G

20630418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713095-A-G

20630986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713471-G-C

20630986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713471-G-T

20631004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57713488-T-C

20631172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713645-A-G

20631173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713646-T-C

http://identifiers.org/hco/13/GRCh38#20631220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57713694-C-A

20631220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713694-C-T

20631246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713718-G-T

20631422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713864-A-G

20631453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713880-A-G

20631483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713910-G-A

20631483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713910-G-C

20631483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713910-G-T

20631492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713918-T-A

20631492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713918-T-C

20631492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57713918-T-G

20637870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57714920-G-A

20638264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57715285-G-A

20638264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57715285-G-T

20638397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57715413-A-G

20638406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57715422-T-C

20638458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57715474-G-A

20639476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57716555-T-G

20639561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57716593-C-G

20641246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57717325-A-G

20641246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57717325-A-T

20641249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57717328-A-G

20641274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57717348-T-C

20641307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57717371-C-T

20641309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57717373-A-G

20641351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57717415-C-T

20641354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57717418-A-G

20641372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57717436-C-T

http://identifiers.org/hco/13/GRCh38#20641415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57717478-C-A

20641495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717543-G-A

20641495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717543-G-T

20641579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717602-T-A

20641634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717697-G-C

20641634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717697-G-T

20641641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717707-A-T

20641789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717818-A-G

20642013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57717991-C-T

20643633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718292-G-A

http://identifiers.org/hco/13/GRCh38#20643741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57718396-A-C

20644716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718746-G-A

20644716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718746-G-C

20644716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718746-G-T

20644756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718786-A-G

20644798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718810-G-A

20644798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57718810-G-T

20644869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57718879-T-C

20644869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57718879-T-G

http://identifiers.org/hco/13/GRCh38#20645039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57719045-C-A

20645039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57719045-C-T

20646659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720360-A-G

http://identifiers.org/hco/13/GRCh38#20646729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57720422-A-C

20646729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720422-A-T

20646751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720447-T-C

20646865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720571-C-T

20646877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720583-C-T

20647173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57720947-T-G

20647804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57721753-C-T

20648134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57722032-T-G

20648170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57722068-C-G

20648170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57722068-C-T

20653205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724728-T-G

20653807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724954-A-G

20653807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724954-A-T

20653824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724975-A-G

20653830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724981-A-G

20653830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724981-A-T

20653840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57724993-T-G

20653860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725013-T-C

20653860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725013-T-G

20653869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57725022-T-C

20653922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57725075-A-G

20653960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725113-T-A

20653960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725113-T-C

20654000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725153-G-T

20654007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725160-A-G

http://identifiers.org/hco/13/GRCh38#20654079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57725235-C-A

20654081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725237-A-G

20654727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725779-A-G

20654739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725791-A-T

http://identifiers.org/hco/13/GRCh38#20654779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57725846-A-C

20654779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57725846-A-G

http://identifiers.org/hco/13/GRCh38#20656216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57726171-C-A

20656216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726171-C-G

20656216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726171-C-T

20656298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726269-T-C

http://identifiers.org/hco/13/GRCh38#20656348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57726331-C-A

20656348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726331-C-T

20656382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57726366-T-C

20656417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57726401-A-G

20656417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57726401-A-T

20656449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726433-T-C

20656511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726490-G-T

20656566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57726540-T-C

20657371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57727077-A-G

20657681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57727265-A-G

20663056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57733022-G-A

http://identifiers.org/hco/13/GRCh38#20663243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57733246-C-A

20663243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733246-C-T

http://identifiers.org/hco/13/GRCh38#20663334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57733318-C-A

20663334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733318-C-T

http://identifiers.org/hco/13/GRCh38#20663351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57733335-A-C

20663356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733340-G-A

20663397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733399-T-G

20663482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733617-A-G

20663482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57733617-A-T

20667318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739249-A-G

20667358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739293-G-A

20667358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739293-G-T

20667945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740484-C-T

20668018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740538-C-G

20668092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740608-T-C

20670499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57744232-A-T

20670782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57744493-G-A

20670874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57744560-G-C

20670874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57744560-G-T

20671042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57744731-A-T

20671467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57745100-T-C

20671523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57745156-T-C

20671648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57745277-C-G

20672209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57745686-C-G

20672456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57745887-C-G

http://identifiers.org/hco/13/GRCh38#20672469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57745895-C-A

20673036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57746587-G-A

20673116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57746654-G-A

20673408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57746991-T-A

20673541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57747091-G-A

20673568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57747117-A-G

20673905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57747343-T-C

http://identifiers.org/hco/13/GRCh38#20674266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57748843-C-A

20674574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749139-G-T

20675173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749404-A-G

20675283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749510-A-G

20675283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749510-A-T

20675828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749926-T-C

20675898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57749981-G-T

20675981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57750056-G-C

20676166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57750238-G-C

20677074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57750965-C-T

20677891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751418-G-A

20677930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751462-G-A

20678027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751564-T-C

20686069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752701-T-C

http://identifiers.org/hco/13/GRCh38#20686148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57752777-A-C

20686148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752777-A-G

http://identifiers.org/hco/13/GRCh38#20686747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57753253-C-A

20690743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57754476-C-G

20690743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 57754476-C-T

20690846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754591-A-G

20690847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754592-T-C

20690847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754592-T-G

20690848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754593-A-T

20690867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754615-G-A

http://identifiers.org/hco/13/GRCh38#20691121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#57754861-C-A

20691121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57754861-C-T

20691210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57755244-G-A

20691210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57755244-G-T

20691250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57755283-A-G

20691330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20606
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57755360-T-C