http://identifiers.org/hco/10/GRCh38#104129950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47726011-C-A

104129951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726012-A-G

http://identifiers.org/hco/10/GRCh38#104130018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47726050-C-A

104130018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726050-C-T

104130021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726053-G-A

104130021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726053-G-T

104130045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726076-A-G

http://identifiers.org/hco/10/GRCh38#104130056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47726087-A-C

104130100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726124-A-T

104130110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726137-T-C

104130110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3 prime UTR variant
orthologous variants: 47726137-T-G

http://identifiers.org/hco/10/GRCh38#104130347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47726367-A-C

104130347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726367-A-G

104130370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726388-T-G

104130383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726401-T-A

104130383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726401-T-C

104130384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726402-G-A

104130384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726402-G-T

104131483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 47726620-A-G

http://identifiers.org/hco/10/GRCh38#104131618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47726744-C-A

104131618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47726744-C-T

104131877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727003-C-T

104132075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727175-A-T

104132286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727393-T-G

104132307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727412-G-A

104132307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727412-G-T

104132317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727422-A-T

104133362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727866-T-A

104133362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47727866-T-C

104133490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47728009-A-G

104133490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47728009-A-T

http://identifiers.org/hco/10/GRCh38#104133503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47728023-C-A

104133503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47728023-C-T

104133524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47728044-T-C

104133752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47728241-C-T

104140313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47733268-C-T

104140436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47733386-G-A

104140436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47733386-G-T

104141136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734172-G-A

104141136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734172-G-T

104141642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734444-T-C

104141642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734444-T-G

104141705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734500-T-C

104141756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734551-T-A

http://identifiers.org/hco/10/GRCh38#104141988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47734768-C-A

104141996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734778-C-G

104142072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734855-A-T

104142156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734936-A-G

http://identifiers.org/hco/10/GRCh38#104142160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47734944-C-A

104142160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734944-C-T

104142161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734945-A-G

104142167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734951-G-A

104142167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47734951-G-T

104142236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47735024-A-G

http://identifiers.org/hco/10/GRCh38#104142258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47735047-C-A

104142258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47735047-C-T

104142324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47735111-T-C

104142422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735207-G-T

104142431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735216-G-A

104142431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735216-G-C

104142431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735216-G-T

104142517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735296-C-T

104142698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735512-A-G

104142720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47735533-G-T

104143107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47736000-T-C

104143382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47736238-A-G

104143388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47736244-G-A

104143401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47736258-T-C

104143513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47736368-A-G

104143516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47736371-G-C

104143694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47737103-T-A

104143694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47737103-T-C

104143763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47737169-T-A

http://identifiers.org/hco/10/GRCh38#104143780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47737186-C-A

104143930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47737365-G-A

104144925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47738791-G-A

104145057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47738915-G-A

http://identifiers.org/hco/10/GRCh38#104145279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47739095-C-A

104145349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739181-T-A

http://identifiers.org/hco/10/GRCh38#104145437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47739279-C-A

104145437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739279-C-T

104145584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739641-T-C

104145608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739665-A-G

104145628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739685-T-A

104145628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739685-T-C

104145628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739685-T-G

http://identifiers.org/hco/10/GRCh38#104145635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47739692-C-A

http://identifiers.org/hco/10/GRCh38#104145665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47739722-A-C

104145665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47739722-A-G

104145989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740015-G-A

104146005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740031-T-C

104146162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740168-A-T

104146186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740192-A-G

http://identifiers.org/hco/10/GRCh38#104146419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47740420-C-A

104146419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740420-C-G

104146419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740420-C-T

104146433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740434-G-T

104147354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47740868-C-T

http://identifiers.org/hco/10/GRCh38#104147447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47740958-A-C

104147533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741044-T-C

104147807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741341-G-A

104147807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741341-G-T

104147809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741343-G-T

104147813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741347-A-G

104147813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741347-A-T

http://identifiers.org/hco/10/GRCh38#104147817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47741351-A-C

104147828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741362-T-C

104148017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741541-A-G

104148021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741545-G-A

104148021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741545-G-C

104148021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741545-G-T

104148079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741617-G-T

104148094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741636-A-G

104148123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741655-A-G

104148142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741674-T-A

104148372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47741900-C-T

104152711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47744545-G-T

104152786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47744599-A-T

104152807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47744620-G-A

104152807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47744620-G-C

104152807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47744620-G-T

http://identifiers.org/hco/10/GRCh38#104152814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47744627-C-A

104152814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47744627-C-T

104160745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47746194-G-C

104160799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47746248-G-A

http://identifiers.org/hco/10/GRCh38#104160889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47749174-C-A

104160889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749174-C-T

http://identifiers.org/hco/10/GRCh38#104160931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47749216-C-A

104160931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749216-C-T

http://identifiers.org/hco/10/GRCh38#104161027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47749292-C-A

104161094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47749355-G-A

104161094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47749355-G-T

104161213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749440-A-G

104161282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749476-G-A

104161282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749476-G-C

104161296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749490-A-G

104161865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749985-T-A

104161865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47749985-T-C

104162015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47750130-C-G

http://identifiers.org/hco/10/GRCh38#104162053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47750168-C-A

104162053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750168-C-T

104162088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750203-A-T

http://identifiers.org/hco/10/GRCh38#104162101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47750216-C-A

104162101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750216-C-T

104162151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750249-G-A

104162151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750249-G-T

104162187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750285-A-T

104162217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750311-G-T

104162282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750351-G-C

104162285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750354-T-A

104162285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750354-T-C

104162309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47750373-C-T

104162318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 47750382-T-C

104162327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47750391-A-G

104162367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47750437-C-T

104162479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750554-G-A

http://identifiers.org/hco/10/GRCh38#104162483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47750558-C-A

104162483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750558-C-T

104162515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750590-G-A

104162515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750590-G-T

104162942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47750992-T-C

104163037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751096-C-G

104163037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751096-C-T

104163142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751190-G-C

104163142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751190-G-T

104163156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751205-G-A

104163158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751207-C-T

104163422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751432-T-G

104163454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751462-C-G

104163498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751502-T-G

104163729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751715-A-G

104163843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751824-G-C

104163925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47751904-G-A

http://identifiers.org/hco/10/GRCh38#104163956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47751934-C-A

http://identifiers.org/hco/10/GRCh38#104163968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47751946-C-A

104164073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752059-G-A

104164073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752059-G-C

104164151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47752137-T-C

104164220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47752206-G-A

104164358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752346-T-C

104164358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752346-T-G

http://identifiers.org/hco/10/GRCh38#104164363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47752351-C-A

104164381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752362-T-A

104164381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752362-T-C

104164381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752362-T-G

104165189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752849-C-G

104165189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47752849-C-T

104165555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47753451-T-C

104165859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47753699-C-T

104166045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47753872-A-G

104166350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754101-G-A

104166350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754101-G-C

104166423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754145-A-G

104166445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754167-G-A

104166445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754167-G-C

104166445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754167-G-T

104166485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754236-C-T

104166624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47754375-G-A

104166624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47754375-G-C

http://identifiers.org/hco/10/GRCh38#104166662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47754413-A-C

104166662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47754413-A-G

104166663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47754414-T-C

104166745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754499-A-G

104166745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754499-A-T

http://identifiers.org/hco/10/GRCh38#104166844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47754596-A-C

104167168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47754906-T-C

104167376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47755119-C-G

104167399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47755143-T-G

104167467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47755205-G-A

104167467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47755205-G-T

104167606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47758801-T-C

104167632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47758830-C-G

104167633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47758831-T-C

104167633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47758831-T-G

104167687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47758885-C-G

104167687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47758885-C-T

104167740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47758938-T-C

104167790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758986-G-A

104167790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758986-G-T

104167793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758989-T-A

104167793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758989-T-C

104167802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758998-G-A

104167802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47758998-G-T

104167856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759053-T-C

104167915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759097-T-C

104168275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759448-A-G

104168372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759531-C-T

http://identifiers.org/hco/10/GRCh38#104168433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47759591-C-A

104168592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759792-G-A

104168592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759792-G-C

104168592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759792-G-T

104168608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759863-A-G

104168659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759901-A-G

104168659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759901-A-T

104168662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759904-T-A

104168678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759916-T-A

104168678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759916-T-G

104168691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759935-A-G

http://identifiers.org/hco/10/GRCh38#104168711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47759955-A-C

104168711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759955-A-G

104168726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759975-T-C

104168727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759976-A-G

104168728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47759977-G-T

104168911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760135-T-C

104168915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760139-T-C

http://identifiers.org/hco/10/GRCh38#104168929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47760152-A-C

104168929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760152-A-G

http://identifiers.org/hco/10/GRCh38#104168959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47760181-A-C

http://identifiers.org/hco/10/GRCh38#104168976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47760202-C-A

104168976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760202-C-T

http://identifiers.org/hco/10/GRCh38#104168994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47760220-A-C

http://identifiers.org/hco/10/GRCh38#104169122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47760343-C-A

104169171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760382-G-A

104169344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760597-C-T

104169354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760607-G-A

104169633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47760884-A-G

104169910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47761088-C-G

104170039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47761213-G-C

http://identifiers.org/hco/10/GRCh38#104170160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47761322-A-C

104172437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47761489-A-G

104172455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47761507-C-T

http://identifiers.org/hco/10/GRCh38#104172581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47761633-C-A

104172581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47761633-C-G

104172581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47761633-C-T

104176070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47762919-T-A

104176202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47763057-T-C

104176583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47763734-A-T

104178773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47764229-A-T

104178781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47764237-G-T

104178934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47764361-G-A

104178934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47764361-G-T

104179130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47764560-T-A

http://identifiers.org/hco/10/GRCh38#104179361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47766176-A-C

104179446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47766234-G-A

104179628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47766404-G-A

104179708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47766450-G-T

104179881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47766871-C-T

http://identifiers.org/hco/10/GRCh38#104179884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47766874-C-A

104179884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47766874-C-T

104179890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47766877-G-C

104182231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768583-T-C

104182247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768600-G-T

http://identifiers.org/hco/10/GRCh38#104182392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47768732-C-A

104182392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47768732-C-T

104182440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47768777-T-C

104182534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768871-A-G

104182540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768877-A-G

104182540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768877-A-T

104182546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768910-T-A

104182546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768910-T-C

http://identifiers.org/hco/10/GRCh38#104182547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47768911-A-C

104182547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768911-A-G

104182604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47768957-T-C

104183305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47769605-C-T

104184627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770391-C-T

104184714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770474-C-T

104184916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770646-G-T

104184934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770664-C-T

104184978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770684-T-C

104184991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770697-G-T

104185183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770886-T-C

104185183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770886-T-G

http://identifiers.org/hco/10/GRCh38#104185224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47770949-C-A

104185224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47770949-C-G

104185529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47771248-G-A

104185583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47771300-A-G

http://identifiers.org/hco/10/GRCh38#104185705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47771428-A-C

104185855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47771585-T-G

104185861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47771591-T-C

http://identifiers.org/hco/10/GRCh38#104186162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47773908-C-A

104186162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773908-C-G

104186177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773926-T-A

104186177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773926-T-G

104186191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773943-T-C

104186198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773950-G-T

http://identifiers.org/hco/10/GRCh38#104186199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47773951-C-A

104186199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773951-C-T

104186206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773958-T-C

104186206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773958-T-G

104186257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47773988-T-C

104186559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47774614-G-A

104186954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775029-G-A

104187144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775205-T-C

104187182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775249-G-A

104187182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775249-G-T

http://identifiers.org/hco/10/GRCh38#104187259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47775326-A-C

104187259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775326-A-G

104187259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775326-A-T

http://identifiers.org/hco/10/GRCh38#104187272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47775333-A-C

104187311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775351-T-C

104187413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47775453-A-G

104187446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47775486-G-C

104187449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47775489-T-C

104187516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775555-G-A

104187516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775555-G-T

http://identifiers.org/hco/10/GRCh38#104187523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47775562-C-A

104187523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775562-C-T

104187526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775617-G-A

104187526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47775617-G-T

http://identifiers.org/hco/10/GRCh38#104188050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47776537-C-A

104188070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47776578-C-T

104188107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47776613-C-T

http://identifiers.org/hco/10/GRCh38#104188152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47776659-C-A

104188249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47776731-G-A

104188249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47776731-G-T

104188284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47776765-G-A

104188306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47776787-A-G

104188369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47776850-A-G

104188517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47777098-T-G

104188887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47777664-A-G

104189041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47777777-A-G

104189247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47777948-T-A

104189472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47778138-A-G

104189544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47778197-C-G

104189544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47778197-C-T

104189690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47778326-C-T

104190409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779029-C-T

104191752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779427-T-A

104191790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779465-G-A

104191790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779465-G-C

104191790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779465-G-T

104192074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779738-G-T

104192086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779751-G-T

104192101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779766-A-G

104192150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779804-T-C

104192339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47779999-G-T

http://identifiers.org/hco/10/GRCh38#104192410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47780097-C-A

104192410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47780097-C-T

http://identifiers.org/hco/10/GRCh38#104192431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47780208-C-A

104192477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47780253-G-T

104192485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47780261-G-A

http://identifiers.org/hco/10/GRCh38#104192507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47780283-C-A

104192520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47780289-T-C

104193273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783391-A-G

104193293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783410-G-T

104193295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783412-G-C

104193295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783412-G-T

104193337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783442-G-T

http://identifiers.org/hco/10/GRCh38#104193438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47783538-C-A

http://identifiers.org/hco/10/GRCh38#104193494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47783599-C-A

104193701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783899-C-G

104193701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47783899-C-T

104193824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47784003-G-A

104193857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47784033-A-G

104193943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47784119-G-A

http://identifiers.org/hco/10/GRCh38#104193998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47784174-C-A

http://identifiers.org/hco/10/GRCh38#104194066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47784232-A-C

104195189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47784528-G-A

http://identifiers.org/hco/10/GRCh38#104195316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47784762-A-C

104195316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47784762-A-G

104195319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47784770-G-A

http://identifiers.org/hco/10/GRCh38#104195909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47785249-A-C

104196802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47785500-T-C

http://identifiers.org/hco/10/GRCh38#104196819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47785514-A-C

http://identifiers.org/hco/10/GRCh38#104197826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47790205-C-A

104197826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47790205-C-T

http://identifiers.org/hco/10/GRCh38#104197830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47790209-C-A

104197830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47790209-C-T

http://identifiers.org/hco/10/GRCh38#104197865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47790244-A-C

http://identifiers.org/hco/10/GRCh38#104197892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47790268-C-A

104197892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47790268-C-T

104197898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47790274-G-A

104197898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47790274-G-T

104197924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 47790304-T-C

104198004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47790384-G-A

104198119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47790493-T-A

104198178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47790545-T-C

104202713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47792335-T-C

104202714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47792336-A-G

104202845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47792458-G-T

http://identifiers.org/hco/10/GRCh38#104202929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47792524-A-C

104203176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47792714-C-T

104203354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47800201-T-G

http://identifiers.org/hco/10/GRCh38#104203366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47800212-C-A

104203410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47800258-T-C

104203410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47800258-T-G

104203443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800295-G-A

104203443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800295-G-T

http://identifiers.org/hco/10/GRCh38#104203454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47800306-C-A

104203496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800343-A-G

104203518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800365-G-T

104203617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800465-G-A

104203617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800465-G-T

104203647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47800486-A-T

104203771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47800606-A-G

http://identifiers.org/hco/10/GRCh38#104203866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47800687-A-C

http://identifiers.org/hco/10/GRCh38#104203893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47800705-C-A

104203893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47800705-C-T

104203923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47800728-T-C

104204207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801073-C-T

104204530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801368-T-C

104204681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801460-T-C

104205258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801741-T-A

104205299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801782-A-G

104205422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801849-T-A

104205422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47801849-T-C

104205636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802006-G-C

104205662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802031-C-G

104205725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802100-T-A

104205824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802202-G-A

104205824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802202-G-C

104205824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802202-G-T

http://identifiers.org/hco/10/GRCh38#104205839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47802217-A-C

104205839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802217-A-G

104205909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802293-T-C

104205944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47802348-G-T

104206037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47802441-G-A

104206350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47803208-G-T

104206474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47803329-G-T

104206616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47803441-G-A

104207450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47803954-C-T

104207503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804004-T-C

104207523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804069-A-T

104207534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804080-A-G

104207534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804080-A-T

104207594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804151-G-A

http://identifiers.org/hco/10/GRCh38#104207624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47804214-C-A

104207624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804214-C-T

104207629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804219-G-A

104207629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47804219-G-T

http://identifiers.org/hco/10/GRCh38#104207822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47804409-C-A

104207822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47804409-C-T

104208585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47807666-G-C

104208586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47807667-G-C

http://identifiers.org/hco/10/GRCh38#104208635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47807719-C-A

104208818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47807906-A-G

104210300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47809865-C-G

104210399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47809919-C-T

104210467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47809972-A-G

104210528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810002-A-G

104210568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810039-G-C

104210710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810172-A-G

104210744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810206-T-C

104210764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810227-T-C

104211377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810823-G-A

104211396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810842-A-G

104211416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47810880-T-C

104211668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47811134-C-T

104211678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47811144-T-A

http://identifiers.org/hco/10/GRCh38#104211901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47811390-C-A

104211911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47811399-C-T

104212063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47811524-C-T

104212118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47811579-A-G

104212133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47811594-A-G

http://identifiers.org/hco/10/GRCh38#104212287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47811800-C-A

104212619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47812090-T-C

104212660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47812137-T-C

104212856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47813137-T-C

104212911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47813189-T-G

104213117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47813389-T-A

104213145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47813416-A-G

104213423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47813669-C-T

104214158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814090-T-C

104214159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814091-G-A

104214159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814091-G-T

http://identifiers.org/hco/10/GRCh38#104214194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47814138-C-A

104214194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814138-C-T

104214306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47814248-G-A

104214440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814382-A-G

104214470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814415-T-A

http://identifiers.org/hco/10/GRCh38#104214507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47814454-C-A

104214507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814454-C-T

104214524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814471-T-C

104214524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814471-T-G

104214550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814496-G-A

104214550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814496-G-T

104214560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814506-T-A

104214573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814519-T-A

104214573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814519-T-C

104214578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814524-A-T

104214800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47814714-G-T

http://identifiers.org/hco/10/GRCh38#104220450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47816649-C-A

104220572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47816729-A-G

104220757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47816891-C-T

104220830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47816957-G-A

104220860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47816984-T-C

104220896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47817020-C-T

http://identifiers.org/hco/10/GRCh38#104224783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47818127-A-C

104224783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818127-A-G

104224808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818159-C-G

104224858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818208-C-T

104225080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818452-A-G

104225323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818662-A-T

104225331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818670-T-A

http://identifiers.org/hco/10/GRCh38#104225346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47818687-C-A

104225346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818687-C-T

104225378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818719-G-A

104225378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818719-G-C

104225378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818719-G-T

http://identifiers.org/hco/10/GRCh38#104225468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47818830-C-A

104225468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: missense variant
orthologous variants: 47818830-C-T

104225544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: synonymous variant
orthologous variants: 47818906-C-T

http://identifiers.org/hco/10/GRCh38#104225653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47818995-C-A

http://identifiers.org/hco/10/GRCh38#104225655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47818997-C-A

104225655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47818997-C-T

http://identifiers.org/hco/10/GRCh38#104225822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47819235-C-A

104225822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47819235-C-T

104226443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47819991-T-G

104226494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47820040-C-T

104226510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47820045-G-T

104227155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47820575-T-C

104227217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47820680-A-G

http://identifiers.org/hco/10/GRCh38#104227256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47820705-A-C

http://identifiers.org/hco/10/GRCh38#104227400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47820829-A-C

104227414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47820842-C-T

104228205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47821416-T-C

104228727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47821908-T-C

104228757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47821963-T-C

104228796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47822002-T-C

http://identifiers.org/hco/10/GRCh38#104229018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47822217-C-A

104229018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47822217-C-T

104229952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47823247-A-G

104229978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47823273-T-G

http://identifiers.org/hco/10/GRCh38#104230338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47823688-A-C

104230408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47823744-T-C

104230876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824289-T-A

104230876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824289-T-C

http://identifiers.org/hco/10/GRCh38#104230879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47824292-A-C

104230879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824292-A-G

104230879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824292-A-T

104230880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824293-T-C

104230938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824355-T-C

104230950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47824367-T-G

104231609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825156-G-A

104231632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825162-C-G

104231632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825162-C-T

104231676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825204-A-G

104231716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825234-T-C

104232031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825521-A-G

104232035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825525-T-C

104232035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825525-T-G

104232037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825530-A-G

104232037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825530-A-T

http://identifiers.org/hco/10/GRCh38#104232054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47825549-C-A

104232054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825549-C-T

104232060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825555-G-A

104232060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron_variant, undefined
orthologous variants: 47825555-G-T

http://identifiers.org/hco/10/GRCh38#104232116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47825598-A-C

104232116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825598-A-G

104232116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825598-A-T

104232129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825609-G-A

104232129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825609-G-T

104232153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: intron variant
orthologous variants: 47825629-G-T

104232278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825771-G-A

104232278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825771-G-T

104232280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825773-G-A

104232280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825773-G-T

104232322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825817-G-A

104232322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825817-G-T

http://identifiers.org/hco/10/GRCh38#104232336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47825835-C-A

104232336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825835-C-T

http://identifiers.org/hco/10/GRCh38#104232358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47825857-C-A

104232358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825857-C-G

104232358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825857-C-T

http://identifiers.org/hco/10/GRCh38#104232359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47825858-C-A

104232359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825858-C-G

104232359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26684
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47825858-C-T