14884305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047445-G-C

14884305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047445-G-T

14884307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047447-A-G

14884348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047490-G-A

14884367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047509-G-T

14884405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047521-G-T

14884409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047525-G-A

14884409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047525-G-T

14884489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047584-G-A

14884489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141047584-G-T

http://identifiers.org/hco/20/GRCh38#14885486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141048027-C-A

14885511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048053-G-A

14885692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048229-A-G

14885913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048474-C-T

14885942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048503-G-C

14886239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141048776-G-A

14886480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049208-C-G

14886554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049278-C-T

14886659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049378-C-G

14886732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049453-G-A

14886920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049638-C-G

14886947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049666-G-A

14886947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049666-G-T

14887180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049905-T-G

14887236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141049956-G-A

http://identifiers.org/hco/20/GRCh38#14887239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141049959-C-A

14887826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141050756-G-A

14887826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141050756-G-C

http://identifiers.org/hco/20/GRCh38#14887844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141050774-C-A

http://identifiers.org/hco/20/GRCh38#14887860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141050788-C-A

http://identifiers.org/hco/20/GRCh38#14887991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141050912-C-A

14887991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141050912-C-T

http://identifiers.org/hco/20/GRCh38#14888136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051067-C-A

14888136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141051067-C-T

14888218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051109-A-G

14888267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051158-A-G

http://identifiers.org/hco/20/GRCh38#14888268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051159-C-A

http://identifiers.org/hco/20/GRCh38#14888316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051201-C-A

http://identifiers.org/hco/20/GRCh38#14888361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051218-C-A

14888361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051218-C-T

14888376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051233-G-C

14888376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051233-G-T

14888396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051253-G-A

14888396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051253-G-T

http://identifiers.org/hco/20/GRCh38#14888401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051258-C-A

14888401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051258-C-T

14888539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051373-G-T

14888577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051403-A-G

14888587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051413-A-G

14888587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051413-A-T

14888657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051502-G-A

14888661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141051506-G-C

14888686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051531-G-T

http://identifiers.org/hco/20/GRCh38#14888695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051540-C-A

14888697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051542-G-T

14888708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051553-C-T

14888741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051586-A-G

http://identifiers.org/hco/20/GRCh38#14888789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051634-C-A

14888801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051646-T-C

http://identifiers.org/hco/20/GRCh38#14889112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141051942-C-A

14889159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141051989-T-C

14889285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141052116-T-A

14889320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141052150-G-A

14889592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141052395-G-C

14889606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141052409-C-T

14889683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141052474-T-C

14890319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141053267-G-C

http://identifiers.org/hco/20/GRCh38#14890869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141053463-C-A

14891214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141053671-A-G

http://identifiers.org/hco/20/GRCh38#14891232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141053689-A-C

14891279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141053736-A-G

14891394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054059-G-A

14891518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054176-A-G

14891642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054295-G-C

14891642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054295-G-T

14891918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054912-C-T

14891957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141054957-T-C

14892046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141055035-C-G

14894089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141055391-A-G

http://identifiers.org/hco/20/GRCh38#14894160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141055455-C-A

14894207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141055479-T-C

http://identifiers.org/hco/20/GRCh38#14895438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141058470-C-A

14895438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058470-C-G

14895449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058480-A-G

14895493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058524-T-A

14895493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058524-T-C

14895556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058587-G-A

14895556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141058587-G-T

14895611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141058640-G-A

14895611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141058640-G-T

14895747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141058929-C-G

14895747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141058929-C-T

14895778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141058960-T-C

14895848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059034-G-A

14895949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059121-T-A

14896509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059383-T-C

14896672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059536-G-A

14896711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059575-T-G

14896768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059631-G-A

http://identifiers.org/hco/20/GRCh38#14896961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141059829-A-C

14897005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059877-G-A

14897051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141059918-T-C

14897134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060001-C-T

14897190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060105-G-A

14897237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060147-T-G

14897303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060213-C-T

14897506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060397-A-G

14897522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060413-A-G

14897702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060588-A-G

14897747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060641-A-T

14897788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060683-G-A

14897891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141060785-C-T

14901895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141061242-G-T

14901896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141061243-G-A

14903660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064166-T-C

http://identifiers.org/hco/20/GRCh38#14903702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141064206-A-C

http://identifiers.org/hco/20/GRCh38#14903923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141064395-C-A

14904081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064541-G-A

14904088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064547-G-C

14904462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064891-T-C

14904494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064920-G-A

14904545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064971-T-A

14904562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064988-A-G

14904567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141064993-C-T

14904579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141065005-T-A

14904579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141065005-T-C

14906801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141065966-T-G

14906866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141066032-A-G

14908724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141066713-G-T

14908941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141066932-G-T

14908974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141066964-G-A

14909045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067038-T-C

http://identifiers.org/hco/20/GRCh38#14909056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141067052-C-A

14909305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067241-T-C

14909333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067269-G-A

14909342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067278-T-G

14909361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067295-T-C

14909515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067415-A-G

14909760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067583-G-A

14910044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141067974-T-C

14910165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068092-T-C

http://identifiers.org/hco/20/GRCh38#14910268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141068192-A-C

14910331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068255-G-T

http://identifiers.org/hco/20/GRCh38#14910360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141068279-C-A

14910428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068342-C-G

14910428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068342-C-T

14910505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068404-A-G

14910540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068440-G-A

14910693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068604-T-G

14910742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068652-C-G

14910742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068652-C-T

http://identifiers.org/hco/20/GRCh38#14911012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141068896-C-A

14911090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141068985-A-G

14911106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141069001-T-C

http://identifiers.org/hco/20/GRCh38#14911252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141069147-A-C

14911854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141069548-G-A

14911902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141069595-T-C

14911994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141069688-G-C

14912588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070586-C-T

14912624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070623-T-A

14912767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070747-T-A

14912767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070747-T-C

14912877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070861-A-G

14912900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070884-C-T

14912935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141070918-G-C

http://identifiers.org/hco/20/GRCh38#14913002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141070985-C-A

14913040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141071024-A-G

14913194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141071134-A-G

14914052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141071670-C-T

http://identifiers.org/hco/20/GRCh38#14914139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141071757-A-C

14914236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141071852-T-C

14914556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072131-T-C

http://identifiers.org/hco/20/GRCh38#14914576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141072146-A-C

14914576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072146-A-G

14914916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072451-C-T

14914924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072467-A-G

14915097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072579-A-G

14915260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141072745-C-G

14915596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073090-G-A

http://identifiers.org/hco/20/GRCh38#14915991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141073497-C-A

14915991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073497-C-T

http://identifiers.org/hco/20/GRCh38#14916093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141073597-C-A

14916178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073669-T-C

14916237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073724-G-A

14916271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073758-C-T

14916274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073761-T-G

14916351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141073837-G-A

14916764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141074209-G-A

14917085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141074502-C-T

14917380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141074800-T-C

14917444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141074870-A-G

14917519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141074944-C-T

14917889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075312-G-A

14918239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075401-G-C

14918635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075706-G-A

14918635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075706-G-C

14918635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075706-G-T

14918663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141075740-A-T

14918975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076210-A-G

http://identifiers.org/hco/20/GRCh38#14919065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141076300-C-A

14919065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076300-C-T

14919087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076322-C-T

14919102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076337-T-G

14919195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076433-G-T

14919202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076440-A-G

14919229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076467-C-G

14919249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076490-T-G

14919327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076564-C-T

14919392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076627-T-C

http://identifiers.org/hco/20/GRCh38#14919402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141076637-A-C

14919430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076669-T-G

14919480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076719-T-C

14919549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141076790-A-G

14919864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141077063-G-A

14919907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141077117-A-G

14919975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141077221-T-C

http://identifiers.org/hco/20/GRCh38#14920003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141077248-C-A

14920103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141077339-T-C

14920346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141077592-A-G

14921086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141079627-A-G

14921087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141079628-T-C

14921125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141079666-G-A

14921125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141079666-G-C

14921371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141079913-T-C

14921733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141080266-G-A

14921770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141080307-A-G

14921847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141080375-T-A

14921847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141080375-T-C

14922298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141080757-T-G

14922492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141080905-A-G

14922792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141081433-G-T

http://identifiers.org/hco/20/GRCh38#14922801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141081442-A-C

14923735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141083998-G-T

14924667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141084521-G-A

14925314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141085253-A-T

14925421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141085354-T-G

14925529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141085435-C-T

14925756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141085615-T-C

14925802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141085661-A-G

14926089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141085948-G-A

14926089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141085948-G-C

14926560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086398-G-A

14926608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086446-C-T

14926716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086550-C-T

http://identifiers.org/hco/20/GRCh38#14926721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141086555-C-A

14926793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086626-G-T

14926846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086671-G-C

14926929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086748-A-G

14927116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141086922-A-G

http://identifiers.org/hco/20/GRCh38#14927203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141087378-A-C

14927321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141087485-G-C

http://identifiers.org/hco/20/GRCh38#14927532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#141087682-C-A

14927617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141087763-G-A

14927620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141087766-C-T

14927733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141087866-C-T

14927764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141087896-A-T

14928096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141088895-G-A

14928127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141088926-G-A

14928131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141088930-C-T

14928134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141088933-C-T

14928144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141088943-A-T

14928243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141089039-T-A

14928309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141089104-A-G