12575324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29500834-T-C

12575348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29500810-G-A

12575348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29500810-G-C

12575434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29500737-T-A

12582114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29498674-C-G

12582125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29498659-C-T

12582539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29498228-G-T

12582569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29498174-A-T

12587092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29495566-A-T

12587251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29495456-A-G

12588061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29494691-T-C

12592583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29493891-C-G

12593062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29493425-A-G

12593109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29493379-G-A

12593759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29492668-G-A

12593885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29492543-G-A

12594430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29490102-C-T

12595397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29489373-G-A

12596085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29488997-G-A

12628626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29482319-G-C

12628900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29482031-C-T

http://identifiers.org/hco/5/GRCh38#12630126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29481118-C-A

12630212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29481052-A-G

12630240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29481027-G-A

12630339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29480934-T-C

12630353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29480922-G-A

12630363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29480912-A-T

http://identifiers.org/hco/5/GRCh38#12630450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29480824-A-C

12630450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29480824-A-G

12630507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29480775-A-T

12635348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460588-G-A

12635378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460561-C-G

12635409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460531-C-T

12635432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460507-C-T

12635509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460433-A-G

http://identifiers.org/hco/5/GRCh38#12635554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29460378-C-A

http://identifiers.org/hco/5/GRCh38#12635565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29460367-A-C

12635589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29460343-T-A

http://identifiers.org/hco/5/GRCh38#12642228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29454152-C-A

12642228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454152-C-G

12642397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454005-A-G

12642433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453969-A-T

12642532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453888-C-T

12642927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453546-G-A

12649638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29448567-G-C

12649657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29448548-T-G

http://identifiers.org/hco/5/GRCh38#12649682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29448523-C-A

12650159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29448077-T-C

12659493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442845-T-G

12659512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442826-A-G

12659620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442719-A-G

12659736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442609-T-C

12660263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442100-T-C

http://identifiers.org/hco/5/GRCh38#12660330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29442046-A-C

12660342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29442034-A-G

http://identifiers.org/hco/5/GRCh38#12669354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29440144-A-C

12669398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440097-C-G

12669456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440041-A-G

12669663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439819-A-G

12669897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439566-C-T

12670098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439364-A-G

12670113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439334-A-G

12670292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439090-G-A

12670356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29439034-A-G

12670395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438997-A-G

12670796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438662-C-T

12670919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438483-G-A

12670919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438483-G-T

12670980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438445-T-C

12670993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438432-A-G

12671043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438410-C-G

12671104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438357-G-A

12671117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438344-G-T

12671137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438337-G-A

12671188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438292-C-T

12671326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438153-C-G

12675222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29437176-A-G

12693728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29405347-G-A

12693852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29405222-A-G

12693910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29405171-G-A

12693924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29405158-A-T

12694029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404976-T-A

12694029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404976-T-G

12694139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404869-G-T

12695255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404759-C-T

12695483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404518-A-G

12695483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404518-A-T

12695551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404454-T-C

12695559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404445-C-T

12695697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404302-C-T

12695967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403422-C-T

12696006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403383-G-C

12696053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403337-C-T

12696093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403295-G-T

12696162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403227-A-G

12696218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403175-T-C

12696242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403145-A-G

12696257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403130-C-T

12696469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402914-T-C

12696513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402872-T-A

http://identifiers.org/hco/5/GRCh38#12696538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29402773-A-C

12696578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402733-G-A

12696628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402684-A-G

12696940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402387-G-T

12696951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402376-A-T

12696988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402339-A-G

12699828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398484-C-T

12699881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398431-C-G

12699938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398376-A-G

12700124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398088-T-C

12700387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397833-T-G

12701806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388733-T-C

12702133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388396-A-G

12702236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388289-C-G

12704841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379099-C-T

http://identifiers.org/hco/5/GRCh38#12705162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29378883-C-A

12705162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378883-C-T

12705458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378617-C-T

12712210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360571-A-G

http://identifiers.org/hco/5/GRCh38#12712292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29360504-A-C

12712326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360452-A-G

12712582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360175-T-C

12712613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360145-T-C

12712619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360139-A-G

12712825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359926-T-C

12713221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359504-C-G

12713753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359099-T-C

12714303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357965-A-G

12714680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29357508-C-G

12723070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29338822-T-C

http://identifiers.org/hco/5/GRCh38#12723128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29338765-A-C

12723299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29338596-A-T

12723353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29338527-T-C

http://identifiers.org/hco/5/GRCh38#12751605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29327213-C-A

12751815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327041-T-A

12751850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29327002-T-G

12751929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29326929-A-G

12751959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29326900-G-A

12753966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29324407-T-C

12754274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29324212-A-G

12754393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29324074-T-C

12754435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29324032-G-C

12754867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321960-G-A

12756945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321551-T-C

12757188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321306-A-G

12757483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29321003-C-G

http://identifiers.org/hco/5/GRCh38#12757678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29320814-C-A

http://identifiers.org/hco/5/GRCh38#12757796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29320609-A-C

http://identifiers.org/hco/5/GRCh38#12777197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29316999-A-C

12777315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316895-G-A

12777371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316833-T-C

12777387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316817-T-G

http://identifiers.org/hco/5/GRCh38#12777459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29316754-A-C

12777651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316564-T-C

12778416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316146-G-C

12778482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316041-T-C

12778482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316041-T-G

12778494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29316029-A-G

12780782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29309202-G-A

12780820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29309164-C-T

12780912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29309072-A-G

12781216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308815-A-G

12781368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308692-T-C

12781472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308592-C-G

http://identifiers.org/hco/5/GRCh38#12781629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29308465-C-A

12781669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308426-C-T

12781684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308417-G-A

12782096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29308005-C-T

12782215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307878-G-A

12782240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307853-A-G

12782469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307675-G-T

12782487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307657-C-G

12782619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307594-A-G

12782736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307532-C-T

12782879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307403-C-T

12782920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307354-C-G

12783028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307243-C-T

12783262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29307031-A-G

12783495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306870-C-G

12783685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306717-C-T

12784048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306415-G-A

12784048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306415-G-C

http://identifiers.org/hco/5/GRCh38#12784147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29306315-A-C

12784259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306224-T-C

12784411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306068-G-A

12784411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29306068-G-C

12784454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29306009-A-G

12784523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29305930-T-G

12784703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29305757-A-G

12784860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29305611-T-A

12792156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29296756-T-C

12792386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29296421-G-A

12799871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29295235-T-C

http://identifiers.org/hco/5/GRCh38#12800024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#29295075-A-C

12800175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294943-A-G

12800292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294839-A-G

12800421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294702-T-C

12800450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294672-G-A

12800580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294545-T-C

12800615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294510-T-G

12800618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294507-C-G

12800683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294443-A-G

12800687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294439-T-C

12800688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294438-A-G

12800856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29294250-C-G

12803353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29281680-T-C

12803369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29281664-A-G

12803542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29281544-A-G

12803612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29281464-T-C

12803665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29281416-T-A