98731353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47015714-A-G

98731391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47015752-T-C

http://identifiers.org/hco/9/GRCh38#98731586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47015930-C-A

98731614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47015960-T-C

98731615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47015961-G-T

98731649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47015984-G-T

http://identifiers.org/hco/9/GRCh38#98731715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47016017-C-A

98731715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016017-C-T

http://identifiers.org/hco/9/GRCh38#98731750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47016048-C-A

98731750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016048-C-T

98731825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016123-T-C

98731939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016203-T-C

98731989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016275-A-G

98731990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016276-G-A

98731990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016276-G-T

98732004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3 prime UTR variant
orthologous variants: 47016290-G-C

98732026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016311-T-C

http://identifiers.org/hco/9/GRCh38#98732044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47016329-A-C

http://identifiers.org/hco/9/GRCh38#98732106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47016375-A-C

98732106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016375-A-G

98732133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016402-G-A

98732145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016414-T-C

98732249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016515-A-G

98732259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016525-A-G

98732272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016538-G-A

98732272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016538-G-T

98732288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016556-A-G

98732288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016556-A-T

98732291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016559-T-C

98732291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016559-T-G

98732303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016571-A-T

98732314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016582-G-A

98732314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016582-G-T

98732365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016626-A-T

http://identifiers.org/hco/9/GRCh38#98732429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47016689-C-A

98732429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016689-C-T

98732488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47016751-G-A

98732613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47016882-G-A

98732613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47016882-G-C

98732613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47016882-G-T

98732721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47016989-G-T

http://identifiers.org/hco/9/GRCh38#98736462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47017458-C-A

98736488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47017485-G-A

http://identifiers.org/hco/9/GRCh38#98736507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47017503-C-A

98736507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47017503-C-T

98736552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47017548-G-A

http://identifiers.org/hco/9/GRCh38#98736729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47017699-A-C

http://identifiers.org/hco/9/GRCh38#98736755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47017724-C-A

http://identifiers.org/hco/9/GRCh38#98740284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47018626-C-A

98740483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47018846-G-A

98740484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47018847-C-G

98740484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47018847-C-T

98740633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47018925-C-G

98740638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47018929-T-C

98740782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019027-T-C

98740850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019097-T-C

98740963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019412-C-T

98741076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019513-G-A

http://identifiers.org/hco/9/GRCh38#98741401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47019744-C-A

98741416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019761-C-T

98741507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019918-T-C

98741512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019923-T-C

98741553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47019963-G-A

98742653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021323-G-A

98742740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021397-G-A

98742798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021444-G-A

98742861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021498-T-C

98742861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021498-T-G

98743159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021768-T-C

98743203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021807-G-A

98743203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47021807-G-C

98743733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47022245-G-A

98743863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47022357-G-A

98744016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47022481-T-A

98744178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47022604-A-G

98744198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47022620-C-T

98744873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023162-A-G

http://identifiers.org/hco/9/GRCh38#98744874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47023163-A-C

98744899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023183-G-A

http://identifiers.org/hco/9/GRCh38#98745044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47023265-A-C

98745124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023349-C-G

98745470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023632-G-A

98745470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023632-G-C

98745491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023653-G-T

98745607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47023792-C-T

98745613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47023798-T-C

98745678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47023863-G-T

98745685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023870-G-C

98745685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023870-G-T

98745700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47023882-A-G

98745761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023932-A-G

98745776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023944-T-A

98745776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47023944-T-C

98745994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024099-G-A

98745994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024099-G-T

http://identifiers.org/hco/9/GRCh38#98746078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47024155-C-A

98746086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47024164-A-G

98746100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47024178-G-T

98746176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024256-G-T

98746228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024306-T-C

98746229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024307-G-T

98746238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024315-G-T

98746385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024460-G-T

98749574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024553-T-C

98749692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024657-A-G

98749808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024781-G-A

98749808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024781-G-C

98749903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47024839-C-T

98750477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025385-G-A

98750814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025546-C-G

98750900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025581-G-A

98750900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025581-G-T

http://identifiers.org/hco/9/GRCh38#98750914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025595-C-A

98750914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025595-C-T

http://identifiers.org/hco/9/GRCh38#98750936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025620-C-A

98751012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025669-A-G

98751022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47025679-T-C

http://identifiers.org/hco/9/GRCh38#98751126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025786-A-C

98751126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025786-A-G

http://identifiers.org/hco/9/GRCh38#98751128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025788-A-C

98751128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025788-A-G

http://identifiers.org/hco/9/GRCh38#98751161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025838-C-A

98751161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025838-C-T

98751164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025841-T-C

98751193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025862-G-A

98751193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025862-G-T

http://identifiers.org/hco/9/GRCh38#98751234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47025907-C-A

98751234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025907-C-G

98751234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47025907-C-T

98751346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026004-G-C

98751408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026060-C-T

http://identifiers.org/hco/9/GRCh38#98751655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47026243-A-C

98751803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026394-C-G

98751803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026394-C-T

98755862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026650-C-T

http://identifiers.org/hco/9/GRCh38#98755921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47026715-C-A

98755947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026736-G-A

98756076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026852-G-A

98756141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026910-A-G

98756167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47026934-G-A

98756284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027006-G-A

98756354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027036-G-A

98756360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027042-T-C

http://identifiers.org/hco/9/GRCh38#98756511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47027192-C-A

98756511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027192-C-T

98756526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027207-G-A

http://identifiers.org/hco/9/GRCh38#98756532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47027213-C-A

98756532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027213-C-T

98756538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027219-G-T

98756574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027255-A-G

98756684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027362-A-G

98756692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027369-G-A

98756692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47027369-G-T

98765794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47029409-T-C

98766303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47029863-T-C

98766443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47029996-T-C

98766644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030182-T-C

98766778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030310-T-A

98767967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030569-G-A

98767967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030569-G-C

98768029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030619-G-A

98768029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47030619-G-T

98768242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47030843-T-C

98770390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47032627-G-A

98770595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47032829-A-G

http://identifiers.org/hco/9/GRCh38#98770748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47032986-C-A

98770748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47032986-C-T

98770795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033027-T-C

98770918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47033138-A-G

98770933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47033156-A-G

98771002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47033225-T-C

98771259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033420-C-G

98771259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033420-C-T

98771310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033471-C-T

98771519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033620-T-C

98771573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033673-C-T

98771697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033735-C-G

98771697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033735-C-T

98771951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47033937-C-T

98772015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47034000-G-A

98772066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47034047-G-A

98772066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47034047-G-T

98773057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47034977-A-G

98773160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035033-C-T

98773170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035043-T-C

98773241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035089-T-A

98773417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035280-A-G

98773539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035447-G-A

98773794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035641-G-A

98773794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035641-G-T

98773808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035655-T-C

98773813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035660-G-A

98773813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035660-G-T

http://identifiers.org/hco/9/GRCh38#98773862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035700-C-A

98773862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035700-C-G

98773862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035700-C-T

98773865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035704-A-G

http://identifiers.org/hco/9/GRCh38#98773866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035705-A-C

http://identifiers.org/hco/9/GRCh38#98773869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035708-C-A

98773869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47035708-C-T

http://identifiers.org/hco/9/GRCh38#98773941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035780-A-C

98773941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47035780-A-G

98773971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47035810-C-T

98774072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47035911-G-A

98774072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47035911-G-T

98774117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035952-G-T

98774134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035966-G-A

98774134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035966-G-T

98774145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035977-T-A

98774145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035977-T-C

http://identifiers.org/hco/9/GRCh38#98774148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035980-A-C

98774148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035980-A-G

http://identifiers.org/hco/9/GRCh38#98774156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47035986-C-A

98774156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035986-C-T

98774163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035993-C-T

98774164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47035994-T-C

98774173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036003-G-A

98774173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036003-G-T

http://identifiers.org/hco/9/GRCh38#98774175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47036005-C-A

98774175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036005-C-T

98774333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036113-A-T

98774334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036114-G-C

98774395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036144-A-T

98774645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036311-T-C

98774835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036489-T-A

http://identifiers.org/hco/9/GRCh38#98774903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47036564-C-A

98774903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47036564-C-T

98774939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47036600-A-T

98774974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47036652-G-A

98775556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037184-T-C

98775951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037418-C-T

98775952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037419-G-A

98776002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037472-T-G

98776200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037630-T-C

98776268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037700-C-T

98776302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037737-C-G

http://identifiers.org/hco/9/GRCh38#98776363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47037790-C-A

98776378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47037805-A-G

98776784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038102-C-T

98776785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038103-G-A

98776980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038245-G-A

98777022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038277-C-T

98777246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038677-T-G

http://identifiers.org/hco/9/GRCh38#98777293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47038722-C-A

98777309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038738-T-A

98777309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038738-T-G

http://identifiers.org/hco/9/GRCh38#98777311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47038740-C-A

98777311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038740-C-T

http://identifiers.org/hco/9/GRCh38#98777376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47038890-A-C

98777380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47038894-G-A

98777408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47038917-G-A

98777539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039044-G-T

98777545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039050-C-G

98777609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039114-G-C

98777759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039250-G-A

98778065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039541-C-T

http://identifiers.org/hco/9/GRCh38#98778092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47039563-C-A

98778092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039563-C-G

98778092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039563-C-T

http://identifiers.org/hco/9/GRCh38#98778097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47039568-C-A

98778097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039568-C-G

98778097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039568-C-T

98778111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039580-G-T

98778175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039633-A-G

98778246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47039690-G-T

98778326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47039770-G-A

98778326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47039770-G-C

98778465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039905-G-T

http://identifiers.org/hco/9/GRCh38#98778480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47039920-C-A

98778480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039920-C-T

98778501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039938-G-C

98778501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039938-G-T

http://identifiers.org/hco/9/GRCh38#98778537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47039962-C-A

98778537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039962-C-T

98778541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47039966-T-C

98778692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040056-C-T

98778786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040146-G-C

98778851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040209-C-G

98778851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040209-C-T

98778901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040242-T-C

98780050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040910-T-C

98780097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040959-T-A

98780097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040959-T-C

98780121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040983-G-C

98780128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040989-G-A

98780128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040989-G-T

98780135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040996-G-A

98780135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040996-G-C

98780135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47040996-G-T

98780207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47041033-A-G

98780210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47041036-G-A

98780210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47041036-G-C

98780215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47041041-G-A

http://identifiers.org/hco/9/GRCh38#98780357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47041183-C-A

98780357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041183-C-G

98780410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041235-C-T

98780476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041304-G-A

98780476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041304-G-T

98780556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041330-T-G

98780651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47041416-T-C

http://identifiers.org/hco/9/GRCh38#98780718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47041475-C-A

98782024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043187-G-A

98782148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043269-G-C

http://identifiers.org/hco/9/GRCh38#98782327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47043406-A-C

98782327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043406-A-G

98782327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043406-A-T

98782361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043438-G-A

98782361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043438-G-T

http://identifiers.org/hco/9/GRCh38#98782383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47043458-C-A

98782398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47043473-G-A

98782443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47043518-A-G

98783457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47044421-G-A

98783645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044558-A-T

98783663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044574-A-T

http://identifiers.org/hco/9/GRCh38#98783664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47044575-C-A

98783664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044575-C-T

98783750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044658-G-A

98783750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044658-G-T

98783806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044712-T-C

98783806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044712-T-G

http://identifiers.org/hco/9/GRCh38#98783819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47044725-C-A

98783819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044725-C-G

98783819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044725-C-T

98783849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044757-T-G

98783880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044785-C-T

http://identifiers.org/hco/9/GRCh38#98783920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47044799-C-A

98783920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044799-C-T

98783938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044805-G-A

98783938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044805-G-T

98783950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044817-G-A

98783950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47044817-G-T

98784090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47044957-G-A

98784090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47044957-G-T

98784111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47044978-G-A

98784129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47044996-G-A

98784169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045033-A-G

98784169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045033-A-T

98784176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045040-G-T

98784178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045042-C-G

98784178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045042-C-T

98784394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47045193-G-C

98784394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47045193-G-T

98784424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47045217-G-A

98784424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47045217-G-T

98784476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045282-G-A

98784476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045282-G-T

98784578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045592-T-G

98784583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045702-T-C

http://identifiers.org/hco/9/GRCh38#98784605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47045723-C-A

98784605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045723-C-T

98784776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045956-G-T

http://identifiers.org/hco/9/GRCh38#98784814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47045992-A-C

98784814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045992-A-G

98784814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47045992-A-T

http://identifiers.org/hco/9/GRCh38#98784845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
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/4/GRCm39#47046023-A-C

98784845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47046023-A-G

98784933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046111-G-A

98784933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046111-G-C

98784940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046118-G-A

98784940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046118-G-T

http://identifiers.org/hco/9/GRCh38#98784951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046128-C-A

http://identifiers.org/hco/9/GRCh38#98784952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046129-A-C

http://identifiers.org/hco/9/GRCh38#98784977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046147-A-C

98784987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046157-G-C

98784987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046157-G-T

98785012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046182-T-C

http://identifiers.org/hco/9/GRCh38#98785028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046201-C-A

98785028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046201-C-G

98785028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046201-C-T

http://identifiers.org/hco/9/GRCh38#98785047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046220-A-C

98785200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046285-T-C

98785200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046285-T-G

98785219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046304-G-A

98785413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046488-C-T

98785450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046519-C-G

98785458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046526-G-A

http://identifiers.org/hco/9/GRCh38#98785558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046591-C-A

98785558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046591-C-T

http://identifiers.org/hco/9/GRCh38#98785611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47046631-C-A

98785611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046631-C-T

98785654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47046673-G-C

98786853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047404-G-A

98786975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047510-C-T

98787396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047883-T-C

98787402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047889-T-C

98787491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047952-G-A

98787491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47047952-G-T

98789657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048527-T-C

98789765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048628-T-C

98789765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048628-T-G

http://identifiers.org/hco/9/GRCh38#98789795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47048670-C-A

98789795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048670-C-T

http://identifiers.org/hco/9/GRCh38#98789799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47048674-C-A

98789799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048674-C-G

98789799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47048674-C-T

98789917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048812-T-C

98789917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048812-T-G

98789941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048832-G-A

98789941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048832-G-T

http://identifiers.org/hco/9/GRCh38#98789997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47048873-C-A

98790035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048908-T-A

98790055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048928-A-T

98790075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048941-G-A

98790075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47048941-G-T

http://identifiers.org/hco/9/GRCh38#98790114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47049079-C-A

98790114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049079-C-T

http://identifiers.org/hco/9/GRCh38#98790168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47049133-C-A

98790168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049133-C-T

98790186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049151-G-A

98790243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049208-G-A

98790255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049220-C-T

98790315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049280-G-A

98790315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049280-G-C

98790315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049280-G-T

98790420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47049385-C-G

98790468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 47049433-G-A

98790646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049610-G-A

http://identifiers.org/hco/9/GRCh38#98790671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47049637-C-A

98790671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049637-C-T

98790682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049648-A-T

http://identifiers.org/hco/9/GRCh38#98790703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47049671-C-A

98790703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049671-C-G

98790703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049671-C-T

98790710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049678-T-A

98790710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47049678-T-C

98791320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47050398-G-A

98791320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47050398-G-T

98791331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47050407-G-A

98791704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47050734-T-C

98791932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47050962-A-G

98791936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47050966-T-C

98791998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051025-C-G

98792011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051037-G-A

98792011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051037-G-C

98792035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051061-C-T

98792164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051184-T-G

98792185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051203-G-C

98792696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051647-T-C

98792812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051770-C-T

98792862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051824-G-C

98793001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47051964-C-T

http://identifiers.org/hco/9/GRCh38#98793245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47052171-C-A

98793416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47052337-C-T

98793428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47052349-G-A

98794266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47052747-A-T

98794474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47052930-T-G

98794878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47054871-A-G

http://identifiers.org/hco/9/GRCh38#98794884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47054877-C-A

98794960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47054953-G-C

98795285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056243-T-C

98795325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056281-C-T

98795514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47056425-C-T

98795589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47056498-A-T

98795597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47056506-T-C

98795747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056637-C-G

98795849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056752-G-C

98795849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056752-G-T

98795943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47056828-T-G

98796162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47056978-G-A

98796162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 47056978-G-C

98796162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 47056978-G-T

http://identifiers.org/hco/9/GRCh38#98796210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47057026-C-A

98796210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47057026-C-T

http://identifiers.org/hco/9/GRCh38#98796270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47057086-C-A

98796270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47057086-C-T

98796273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47057089-G-A

98796273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47057089-G-C

98796273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 47057089-G-T

98796372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47057173-G-A

98796372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47057173-G-C

98796372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47057173-G-T

98796587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, undefined
orthologous variants: 47057369-G-A

98796587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, undefined
orthologous variants: 47057369-G-T

98796611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron_variant, undefined
orthologous variants: 47057398-G-T

98796642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26724
most severe consequence: intron variant
orthologous variants: 47057423-C-T