http://identifiers.org/hco/7/GRCh38#98291741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144201407-C-A

98291741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201407-C-T

98291790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201448-G-T

http://identifiers.org/hco/7/GRCh38#98292075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144201686-C-A

http://identifiers.org/hco/7/GRCh38#98292490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144201851-A-C

98292490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201851-A-G

http://identifiers.org/hco/7/GRCh38#98292516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144201877-C-A

98292516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201877-C-T

98292569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201943-A-T

http://identifiers.org/hco/7/GRCh38#98292653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144201990-C-A

98292743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202066-A-G

98292744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202067-T-C

98292744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202067-T-G

98292768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202091-T-A

98292768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202091-T-C

98292768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202091-T-G

98292796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202111-G-A

98293032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202295-T-C

98293032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202295-T-G

98293045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202308-T-C

98293146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202407-G-A

98293211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202479-T-C

98293273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202526-G-A

98293273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202526-G-C

98293273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202526-G-T

http://identifiers.org/hco/7/GRCh38#98293350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144202596-C-A

http://identifiers.org/hco/7/GRCh38#98293396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144202647-C-A

98293405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202656-T-G

98293409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202660-A-T

98293512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202758-G-C

98293657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144202998-C-T

http://identifiers.org/hco/7/GRCh38#98293671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144203015-C-A

98293671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203015-C-G

98293671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203015-C-T

98293712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203041-G-C

98293712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203041-G-T

98293720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203049-A-G

98293740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203069-G-C

98293740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203069-G-T

98293744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203073-G-T

98293767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203134-T-C

98293795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203168-C-T

98293812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203191-C-T

http://identifiers.org/hco/7/GRCh38#98293870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144203240-C-A

98293916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203299-T-C

98293917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203300-G-A

98293927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203308-G-A

98293927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203308-G-T

98293934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203316-G-T

http://identifiers.org/hco/7/GRCh38#98293944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144203326-C-A

98293944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203326-C-G

98293944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203326-C-T

98294036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203384-T-C

98294036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203384-T-G

http://identifiers.org/hco/7/GRCh38#98294067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144203411-C-A

98294067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 144203411-C-T

98294109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 144203453-G-A

98294141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203480-G-A

98294151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203490-T-C

98294200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203599-C-T

98294243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203648-T-C

98294243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203648-T-G

98294330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203712-C-T

98294340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203722-A-G

98294439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203854-C-T

98294509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144203917-G-A

http://identifiers.org/hco/7/GRCh38#98294571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144203946-A-C

98294655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204021-G-T

http://identifiers.org/hco/7/GRCh38#98294718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144204078-A-C

98294729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204089-G-T

98294891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204375-C-T

98294956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204485-C-G

98295073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204617-C-T

98295222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204730-G-A

98295276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204792-T-C

98295314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144204823-G-A

98296368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144205643-G-A

98296368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144205643-G-C

98296400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144205674-C-T

98296436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144205704-A-G

98302023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144209969-C-T

98302104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144210051-G-T

98304260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144212659-G-A

98304349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 144212748-G-A

98304424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144212818-C-G

98305605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144213498-A-G

98305665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144213577-C-T

98305671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144213583-C-T

98305732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144213643-A-G

98306153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214119-G-A

http://identifiers.org/hco/7/GRCh38#98306303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144214330-C-A

98306303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214330-C-T

98306313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214336-T-G

98306342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214360-G-T

http://identifiers.org/hco/7/GRCh38#98306357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144214373-C-A

98306379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214396-A-G

98306379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214396-A-T

98306386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214407-C-G

98306386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214407-C-T

98306397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214418-G-C

http://identifiers.org/hco/7/GRCh38#98306612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144214626-C-A

98306615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144214629-T-C

98306617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 144214631-C-T

http://identifiers.org/hco/7/GRCh38#98306619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144214633-C-A

http://identifiers.org/hco/7/GRCh38#98306630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144214644-C-A

98307490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144215150-A-T

98307554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215209-A-G

98307554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215209-A-T

98307643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215291-G-C

98307643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215291-G-T

http://identifiers.org/hco/7/GRCh38#98307724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144215373-A-C

98307724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144215373-A-G

http://identifiers.org/hco/7/GRCh38#98307748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144215397-C-A

98307748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144215397-C-T

98307940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215586-A-G

98308014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215659-C-T

http://identifiers.org/hco/7/GRCh38#98308110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144215921-C-A

98308110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215921-C-T

98308111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215922-A-T

98308172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215980-G-A

98308172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215980-G-T

98308191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144215999-A-T

98308434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216207-G-A

98308577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216358-T-C

98308613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216395-C-T

http://identifiers.org/hco/7/GRCh38#98308644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144216427-C-A

98308644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216427-C-G

98308644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216427-C-T

http://identifiers.org/hco/7/GRCh38#98309566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144216617-C-A

98309566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144216617-C-T

http://identifiers.org/hco/7/GRCh38#98309618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144216669-C-A

http://identifiers.org/hco/7/GRCh38#98310295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144217217-C-A

98310295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144217217-C-G

98310295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144217217-C-T

http://identifiers.org/hco/7/GRCh38#98310297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144217219-C-A

98310297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144217219-C-T

98310431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144217616-A-G

98310485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144217670-G-T

98310621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217808-T-G

98310631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217818-G-A

98310631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217818-G-T

98310663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217847-G-C

98310663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217847-G-T

98310689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217885-T-C

98310720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217929-T-C

98310814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218008-G-A

98310851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218050-A-G

http://identifiers.org/hco/7/GRCh38#98310905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144218128-C-A

98310923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218137-T-C

98310928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218142-T-A

98310928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218142-T-C

98310953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218166-T-G

98310965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218178-T-C

98310966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218179-G-A

98310978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218191-G-A

98310982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218195-G-A

98312011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218710-G-C

98312011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218710-G-T

98312145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144218848-G-A

98312145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144218848-G-C

98312161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144218864-G-T

98312347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144219052-T-C

98312387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144219088-G-A

98312387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144219088-G-T

98312763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144219547-T-G

98313300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144219983-T-C

98313423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144220104-C-T

98314580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144220635-C-T

98314584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144220639-G-A

98314685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144220739-G-A

http://identifiers.org/hco/7/GRCh38#98315433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144221228-C-A

98315433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221228-C-T

http://identifiers.org/hco/7/GRCh38#98315448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144221243-C-A

98315448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221243-C-T

http://identifiers.org/hco/7/GRCh38#98315457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144221251-C-A

98315457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221251-C-T

http://identifiers.org/hco/7/GRCh38#98315598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144221392-A-C

98315598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 144221392-A-G

98315750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144221530-G-C

98315750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144221530-G-T

98315780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144221570-A-G

98315913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144221655-G-A

98315913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144221655-G-C

98317162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222217-T-A

98317234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144222283-T-A

http://identifiers.org/hco/7/GRCh38#98317291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144222340-A-C

98317291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144222340-A-G

98318230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222563-C-T

98318242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222577-C-G

98320038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144222868-G-A

98320040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144222870-G-A

98320151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222988-T-C

98320151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222988-T-G

98320154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222991-A-G

98320161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222998-G-A

98321308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223679-A-G

98321451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223820-C-T

98321609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223961-T-C

98321614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223966-T-C

98321693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144224033-T-C

98322169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144224195-T-C

98322197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144224225-G-T

98322309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224337-C-T

http://identifiers.org/hco/7/GRCh38#98322672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144224651-C-A

98322841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224795-G-A

98322841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224795-G-C

98322841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224795-G-T

98322878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224830-G-A

98322941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224904-G-A

98322941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224904-G-T

98323041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224980-C-T

98323054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224990-G-C

98323054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144224990-G-T

98323097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144225028-G-A

98323097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144225028-G-T

98323454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225347-T-C

98323554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225441-G-T

98323557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225444-G-A

98323557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225444-G-T

98323681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225554-G-A

98323681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225554-G-C

98323710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225580-C-T

98323861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225715-T-C

http://identifiers.org/hco/7/GRCh38#98323989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144225839-C-A

98324010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225860-T-C

98324046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225897-G-A

http://identifiers.org/hco/7/GRCh38#98324092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144225938-C-A

98324092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144225938-C-T

98324571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144226427-A-G

98324937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144226988-C-T

98325816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144227477-G-A

98326486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144228103-A-G

98326880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144228336-A-G

98327834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144228949-G-A

98327864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144228978-G-A

98328004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144229865-G-C

98328064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144229923-A-G

http://identifiers.org/hco/7/GRCh38#98328143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144230212-A-C

98328365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144230356-C-T

98333734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238283-G-A

98333734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238283-G-C

98333734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238283-G-T

98333783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238318-A-G

98334123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144239087-C-T

98334138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144239111-G-A

98334497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240250-A-G

http://identifiers.org/hco/7/GRCh38#98335183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144240294-A-C

98335183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240294-A-G

98335183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240294-A-T

98335192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240303-G-A

98335192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240303-G-T

98335779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144240791-C-T

98339506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242276-C-T

98339542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242311-T-G

98339557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242324-G-A

98339737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242446-C-T

98339770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242475-T-C

98339828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242515-C-T

98339879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242566-G-T

98339905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242593-C-T

98340033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144242878-C-T

http://identifiers.org/hco/7/GRCh38#98340138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144243329-A-C

http://identifiers.org/hco/7/GRCh38#98340221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144243397-A-C

98340986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144244252-G-T

98340990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144244256-T-G

98341077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144244332-T-C

98342901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144247301-C-G

http://identifiers.org/hco/7/GRCh38#98342955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144247350-C-A

98343069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144247398-T-A

98343069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144247398-T-C

98343607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144247554-A-G

98350293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144251671-G-A

98350340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144251737-A-G

http://identifiers.org/hco/7/GRCh38#98350362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144251756-A-C

98350362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144251756-A-T

98351354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252084-C-G

98351354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252084-C-T

98351390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252110-C-G

98351394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252114-A-G

98351712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252404-G-A

98351850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252538-T-C

98351912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252592-C-G

98351912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144252592-C-T

98352763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144254416-T-A

98352801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144254454-C-G

98352847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144254500-G-A

98352946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144254597-C-G

98353181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144254811-G-A

98354329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255026-T-A

98354357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255058-C-T

98354453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255154-G-C

http://identifiers.org/hco/7/GRCh38#98354564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255278-C-A

98354655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255369-C-T

98354789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255511-C-T

98354871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255573-T-A

98354871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255573-T-C

98354887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255589-G-A

http://identifiers.org/hco/7/GRCh38#98354940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255638-C-A

98354940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255638-C-T

98354941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255639-C-T

98354981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255682-T-C

98355008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255705-G-A

98355008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255705-G-C

98355008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255705-G-T

98355022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255719-T-C

98355022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255719-T-G

http://identifiers.org/hco/7/GRCh38#98355039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255736-C-A

98355039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144255736-C-T

http://identifiers.org/hco/7/GRCh38#98355205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255891-A-C

98355205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144255891-A-G

98355211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144255897-T-A

98355211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144255897-T-C

http://identifiers.org/hco/7/GRCh38#98355260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255946-C-A

98355260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144255946-C-T

http://identifiers.org/hco/7/GRCh38#98355333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144255978-C-A

98355408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144256048-T-A

98355408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144256048-T-C

http://identifiers.org/hco/7/GRCh38#98355456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144256120-C-A

98355456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256120-C-G

98355456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256120-C-T

98355457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256121-T-C

98355475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256143-C-T

http://identifiers.org/hco/7/GRCh38#98355523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144256203-C-A

98355523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256203-C-T

98355530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256210-G-A

98355530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256210-G-T

98355541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256250-A-G

http://identifiers.org/hco/7/GRCh38#98355546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144256255-C-A

98355546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144256255-C-T

98357605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144258423-A-G

98357769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144258580-G-A

98357814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144258626-G-A

98358130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144258915-A-T

98358548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144259221-G-C

98358855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144259446-G-A

98359064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144259599-G-A

98359121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144259617-A-G

98359413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260003-C-T

98359427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260019-C-T

98359513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260127-C-T

98359514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260128-G-A

98359514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260128-G-C

98359532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260145-G-A

http://identifiers.org/hco/7/GRCh38#98359550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144260163-C-A

98359555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260168-G-A

98359566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260180-C-T

98359574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260188-T-C

98361663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260574-T-C

98361675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144260586-T-C

98362218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144261221-A-G

http://identifiers.org/hco/7/GRCh38#98362347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144261357-A-C

98362364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144261374-A-G

98362400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144261410-T-G

98362453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144261463-A-G

98362480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144261487-A-G

98362487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144261494-C-G

98362663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144261953-G-A

98368799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267704-C-T

98368826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267736-G-T

98368844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267754-A-T

98368964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267867-C-T

98369000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267906-G-A

http://identifiers.org/hco/7/GRCh38#98369044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144267950-C-A

98369044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267950-C-T

98369087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267983-C-T

98369094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144267990-G-T

98369167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144268283-A-G

98369441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144268520-G-T

98369459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144268538-T-C

98370867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144269666-G-T

98371116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144269909-G-A

98372177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144270352-G-A

98372177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144270352-G-C

98372673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144270788-G-A

98373233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144271080-C-T

98373610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144271867-C-T

http://identifiers.org/hco/7/GRCh38#98373794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144272526-C-A

98373800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272532-T-A

98373800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272532-T-G

98374330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272755-G-C

98374363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272785-C-G

98374387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272809-C-T

98374451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144272872-T-C

98374619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144273013-T-A

98379182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144275155-G-C

98379405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144275369-A-G

98379774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144275735-T-C

98381015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144277687-C-G

98381053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144277723-T-A

98381300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144277973-T-C

98381378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278030-C-T

98381399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278051-T-C

98381598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278255-A-G

98381612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278270-G-A

98381804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278604-T-G

98381840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278637-T-C

98381859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144278656-A-G

http://identifiers.org/hco/7/GRCh38#98382505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144279343-A-C

http://identifiers.org/hco/7/GRCh38#98382518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144279356-A-C

98382768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144279552-T-C

98384328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144280191-T-C

98384361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144280225-T-C

98384634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144280626-A-T

98389148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144282546-T-G

98395948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287253-A-G

98395953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287248-T-C

98395961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287240-T-G

98396000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287201-A-T

98397261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290846-T-C

98397616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291119-C-T

98397735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291212-T-C

98397898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291383-G-A

98398204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291807-T-C

98398234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291941-T-C

98398268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291979-C-G

98398268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291979-C-T

http://identifiers.org/hco/7/GRCh38#98398356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144292025-C-A

98398381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144292062-T-C

98398622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144292687-G-A

98398645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144292710-A-G

98399055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293104-C-G

http://identifiers.org/hco/7/GRCh38#98399201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144293247-C-A

98399201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293247-C-T

98399209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293255-G-A

98399347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293364-G-A

98399358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293375-C-T

98399377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144293403-T-A

98400082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294210-G-A

98400082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294210-G-T

98400103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294230-G-A

98400103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294230-G-C

98400103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294230-G-T

98400105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294232-G-A

98400105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294232-G-T

98400113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294240-T-C

http://identifiers.org/hco/7/GRCh38#98400146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144294275-C-A

98400146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294275-C-T

http://identifiers.org/hco/7/GRCh38#98400169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144294300-C-A

98400169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294300-C-T

98400222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294348-G-A

98400222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144294348-G-T

98400925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294717-G-A

98400925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294717-G-C

98400996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294791-G-A

98400996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294791-G-T

98401055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294842-G-A

98401055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294842-G-C

98401055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21649
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144294842-G-T