53818207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81134196-T-C

53818324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81134314-T-G

53818394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81134398-A-G

53818705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81134682-C-G

http://identifiers.org/hco/13/GRCh38#53818876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81134826-C-A

53819198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135151-T-G

53819217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135169-C-T

53819384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135329-T-C

53819427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135411-A-G

53819443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135427-T-C

53819479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135464-T-C

53819494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135479-C-T

http://identifiers.org/hco/13/GRCh38#53819544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81135531-C-A

53819544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135531-C-T

53819645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135634-A-T

53819651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135640-C-G

http://identifiers.org/hco/13/GRCh38#53819675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81135663-C-A

53819723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135695-T-C

53819757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81135720-T-C

53820676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81137872-G-T

53820695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81137888-C-G

53820695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81137888-C-T

53820731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81137925-G-A

53820778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81137957-T-C

53821035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138207-G-A

53821079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138253-C-T

http://identifiers.org/hco/13/GRCh38#53821100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81138275-C-A

53821196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138380-T-C

53821274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138443-C-T

53821329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138483-A-G

53821511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138660-G-C

53821528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138673-T-G

53821619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81138783-T-A

53822006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81139154-C-G

53822131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81139284-C-T

53822192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81139345-G-A

53822230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81139383-T-C

53822697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81139841-A-G

http://identifiers.org/hco/13/GRCh38#53822895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81140014-C-A

53822895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140014-C-T

53822960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140078-A-T

53823104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140218-G-A

http://identifiers.org/hco/13/GRCh38#53823160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81140276-C-A

53823241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140352-T-C

53824424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140678-A-G

53824558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140828-G-A

53824702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81140967-G-T

53824928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81141162-A-G

53824928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81141162-A-T

53825073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81141517-G-A

http://identifiers.org/hco/13/GRCh38#53825341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81142395-C-A

53825341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81142395-C-G

53825341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81142395-C-T

53825435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81142484-G-T

53825437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81142486-T-C

53825569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81142622-A-G

http://identifiers.org/hco/13/GRCh38#53825866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81142919-C-A

53826055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143094-A-G

53826062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143103-T-G

53826534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143367-C-T

53826691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143519-G-T

http://identifiers.org/hco/13/GRCh38#53826826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81143655-C-A

53826862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143691-G-A

53827096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143934-A-G

53827133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81143971-T-C

53827169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81144000-G-A

53827455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81144292-G-C

53827477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81144314-A-G

53827668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81144536-T-A

53827750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81144728-C-T

http://identifiers.org/hco/13/GRCh38#53827896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81144952-A-C

53828121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81145151-A-G

http://identifiers.org/hco/13/GRCh38#53828144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81145174-C-A

53828222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81145399-A-G

http://identifiers.org/hco/13/GRCh38#53828239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81145417-A-C

53830494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81148972-T-G

53830496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81148974-G-A

53830496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81148974-G-T

53830703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81149217-G-A

53830721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81149233-G-A

53830746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81149254-A-G

53844189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81151575-A-G

53844208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81151598-G-A

53844219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81151609-T-C

http://identifiers.org/hco/13/GRCh38#53844275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81151666-C-A

53844275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81151666-C-T

53844344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 81151726-G-T

http://identifiers.org/hco/13/GRCh38#53844391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81151765-A-C

http://identifiers.org/hco/13/GRCh38#53844399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81151773-C-A

53844401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: non coding transcript exon variant
orthologous variants: 81151775-C-T

http://identifiers.org/hco/13/GRCh38#53844443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81151816-C-A

53844443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81151816-C-T

53844448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81151819-A-G

53844470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81151841-G-A

53844470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81151841-G-T

http://identifiers.org/hco/13/GRCh38#53844479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81151850-A-C

53844479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81151850-A-G

53844631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152011-G-T

53844812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152156-T-G

53844839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152185-C-T

http://identifiers.org/hco/13/GRCh38#53845157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81152473-C-A

53845495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152824-C-T

53845564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152874-C-T

53845592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81152902-G-C

53845817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81153145-T-C

53846172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81153492-T-C

53846228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81153548-A-T

53846575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81153898-A-G

53846575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81153898-A-T

53846612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81153936-T-A

53847712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81154398-G-A

53847726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81154412-C-T

53847889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81154574-T-A

53847973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81154659-A-G

53848157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81154815-C-G

53848590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155157-G-C

http://identifiers.org/hco/13/GRCh38#53848629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81155202-C-A

53848673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155242-T-A

53848708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155275-A-T

53848894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155468-A-G

53848896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155470-C-T

53848963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155499-A-G

53849238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155724-C-G

53849238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155724-C-T

53849437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155909-C-T

53849523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81155994-G-T

53849571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156038-T-C

53849575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156042-T-C

53849893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156672-A-G

53850057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156801-C-T

http://identifiers.org/hco/13/GRCh38#53850059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81156803-C-A

http://identifiers.org/hco/13/GRCh38#53850070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81156814-C-A

53850180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156915-C-T

53850182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81156917-G-T

53851506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162283-C-G

53851965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162405-T-G

53852307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162717-T-C

53852360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162754-G-A

53852534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162952-T-A

53852534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81162952-T-G

53856243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81175351-G-A

53856243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81175351-G-T

53856265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81175371-G-T

53856410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81175501-A-G

53857200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81176297-G-A

53857238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81176344-A-G

http://identifiers.org/hco/13/GRCh38#53857315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81176414-C-A

53857320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81176419-T-G

53859980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178192-G-T

53860198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178434-C-G

53860500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178720-A-G

53860694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178918-T-C

53860726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178948-C-G

53860752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81178974-G-T

http://identifiers.org/hco/13/GRCh38#53860842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81179059-C-A

53861220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81179471-T-C

53861220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81179471-T-G

53861232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81179483-T-C

http://identifiers.org/hco/13/GRCh38#53861240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81179491-C-A

http://identifiers.org/hco/13/GRCh38#53861248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81179499-C-A

53861258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81179507-C-G

http://identifiers.org/hco/13/GRCh38#53861466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81179693-A-C

http://identifiers.org/hco/13/GRCh38#53861783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81180139-C-A

53861825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81180203-C-G

53861843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81180248-T-C

53862165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81180720-C-T

http://identifiers.org/hco/13/GRCh38#53862630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81181440-C-A

53862686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181498-T-A

53862772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181574-C-T

53862781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181583-G-A

53862808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181609-G-A

53863010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181793-G-C

http://identifiers.org/hco/13/GRCh38#53863022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81181805-A-C

53863119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181902-C-T

53863138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181921-T-C

53863167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81181950-C-G

53863289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81182076-T-C

53863614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81182437-G-A

53864286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81183072-A-G

53870579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81183840-T-C

http://identifiers.org/hco/13/GRCh38#53870650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81183906-C-A

53870737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81183990-C-T

53870781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184034-G-C

53871123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184394-A-G

53871148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184427-T-C

53871246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184506-T-A

53871290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184552-G-T

53871690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81184953-T-G

53872102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81185368-C-T

53872132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81185391-T-A

53872160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81185410-C-T

53872963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81186270-A-G

53873140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81186418-G-A

http://identifiers.org/hco/13/GRCh38#53873247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81186518-C-A

53873437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81186712-T-C

53875925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81191068-T-A

53876107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81191238-T-C

53876115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81191246-T-C

http://identifiers.org/hco/13/GRCh38#53876235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81191371-C-A

53876713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81191878-C-T

53876787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81191953-A-G

53876886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192015-C-T

53876931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192049-C-T

53877028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192136-C-G

53877275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192370-G-A

53877286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192381-A-G

53877305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81192393-T-C

53878609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196130-C-T

53878741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196242-A-G

53879111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196603-T-C

53879132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196624-G-T

53879166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196659-G-A

53879200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196691-G-A

53879200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196691-G-T

http://identifiers.org/hco/13/GRCh38#53879258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81196749-C-A

53879258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196749-C-T

53879331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196822-C-G

53879331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81196822-C-T

53879802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81197299-A-G

http://identifiers.org/hco/13/GRCh38#53879866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81197363-A-C

53880119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81197607-A-G

53880151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81197639-A-G

53880254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81197752-G-A

53880511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81198006-A-G

53880565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81198050-T-C

53886247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208430-T-A

53886247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208430-T-C

53886257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208440-T-A

53886345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208548-G-A

53886469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208687-A-T

53886581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208796-G-C

53886635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208841-T-C

http://identifiers.org/hco/13/GRCh38#53886699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81208900-C-A

53886720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81208920-T-C

http://identifiers.org/hco/13/GRCh38#53886928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81209112-C-A

http://identifiers.org/hco/13/GRCh38#53887339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81209506-C-A

53887342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81209509-G-C

53887456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81209626-T-A

53887595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81209764-T-C

53887595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81209764-T-G

53888317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81210457-A-G

53888451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81210580-G-T

53888825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81210969-T-C

53888883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81210997-G-A

http://identifiers.org/hco/13/GRCh38#53889247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81211351-A-C

53892381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81213078-C-T

53893028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81213682-T-C

53893822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81214471-T-C

53893879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81214525-A-T

53893924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81214566-T-C

53894062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81214711-A-T

53894333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81214961-G-A

53894804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81215408-A-T

http://identifiers.org/hco/13/GRCh38#53895600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81215640-C-A

53895684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81215702-G-A

53895811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81215784-A-G

53895824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81215797-T-C

53896033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81216007-A-G

53896343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81216336-T-C

53897286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81217526-G-A

53897286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81217526-G-T

53897333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81217565-C-T

http://identifiers.org/hco/13/GRCh38#53897340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81217571-C-A

53906056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81223841-T-G

53906421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224140-C-T

53906530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224322-A-G

53906599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224399-T-A

http://identifiers.org/hco/13/GRCh38#53906652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81224459-C-A

53906659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224466-A-G

http://identifiers.org/hco/13/GRCh38#53906674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81224481-A-C

53906920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224706-T-C

53907077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81224846-A-G

53907309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81225104-A-T

53907311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81225106-A-T

53907313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81225108-A-T

53907661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81227371-T-G

53907679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81227391-T-A

53907781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81227478-C-T

53908684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81228401-G-C

53908723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81228440-C-T

53909161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81228860-T-C

53909622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81229889-T-C

53909729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81229991-A-G

53909729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81229991-A-T

53909872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81230121-C-T

53910347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231201-A-G

http://identifiers.org/hco/13/GRCh38#53910380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81231234-C-A

53910502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231330-C-T

53910564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231398-A-G

53910894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231726-T-C

53910931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231763-G-A

53910931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231763-G-T

53911125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81231959-T-G

53911254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232088-A-T

53911307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232137-T-C

53911365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232176-A-G

53911505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232316-G-A

http://identifiers.org/hco/13/GRCh38#53911567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81232379-C-A

53911787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232594-G-T

53911945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232731-T-C

53911971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232762-A-G

53912082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232845-G-A

53912092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81232855-G-A

53912745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81233558-C-T

53912822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81233639-T-C

53913403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81234229-C-T

53913508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81234325-T-C

53913599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81234440-G-A

53914026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81234893-C-T

53914223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235105-G-T

53914325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235198-A-G

53914646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235549-G-T

http://identifiers.org/hco/13/GRCh38#53914694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81235752-C-A

53914694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235752-C-G

http://identifiers.org/hco/13/GRCh38#53914704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81235762-C-A

53914704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235762-C-G

53914896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81235955-T-C

53915051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236103-C-G

53915222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236273-A-G

53915459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236506-A-G

53915536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236574-C-T

53915705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236726-A-T

53915842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236781-C-T

53915918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236851-G-A

53916072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236968-T-C

53916096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81236996-T-C

53916533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237587-C-T

53916622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237681-A-G

53916622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237681-A-T

53916625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237683-G-A

53916625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237683-G-T

53916738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81237794-T-G

http://identifiers.org/hco/13/GRCh38#53916920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81237965-C-A

53917088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81238124-A-G

53917129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81238155-T-C

53917150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81238172-C-T

53917905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81239802-C-T

http://identifiers.org/hco/13/GRCh38#53917971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81239859-C-A

53918188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240189-G-T

53918273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240268-T-C

53918356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240357-C-T

53918385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240427-C-T

53918398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240440-T-C

53918409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240451-G-A

53918431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240473-A-G

53918535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240578-A-G

53918588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240637-A-T

53918627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240671-T-C

53918627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240671-T-G

53918842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240841-C-T

53918847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240846-A-G

53918854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240853-C-T

53918984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81240983-G-A

53919040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81241027-G-A

53919284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81241263-A-G

http://identifiers.org/hco/13/GRCh38#53919426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81241405-C-A

53919475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81241455-G-A

53929486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81244546-A-G

53929511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81244568-A-G

53929513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81244570-C-T

http://identifiers.org/hco/13/GRCh38#53929592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81244647-A-C

53929767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81244840-A-G

53930028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245701-A-G

53930028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245701-A-T

53930035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245708-G-C

53930035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245708-G-T

53930051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245724-G-T

53930052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245725-G-A

53930100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81245757-G-C

53930465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246114-T-C

53930539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246178-G-A

53930585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246222-T-C

53930912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246620-C-T

http://identifiers.org/hco/13/GRCh38#53930914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81246622-A-C

http://identifiers.org/hco/13/GRCh38#53930918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81246626-A-C

53930918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246626-A-G

http://identifiers.org/hco/13/GRCh38#53930925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81246677-A-C

53931088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81246828-C-T

53931591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247217-T-G

53931688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247316-C-G

53931720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247349-G-A

53931832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247461-A-G

53932340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247748-T-C

53932415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81247818-G-C

53932759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248148-A-G

53932767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248156-A-G

53932860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248248-A-T

53932927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248314-C-G

53932935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248322-G-A

http://identifiers.org/hco/13/GRCh38#53933006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81248393-C-A

53933100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248490-T-A

53933317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248708-C-T

53933410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248790-G-T

53933416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81248796-T-G

http://identifiers.org/hco/13/GRCh38#53933597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81248932-A-C

53933689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249033-T-G

http://identifiers.org/hco/13/GRCh38#53933774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81249100-C-A

53933774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249100-C-T

53934012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249326-C-T

53934038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249352-A-G

53934039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249353-C-T

53934118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249427-T-C

http://identifiers.org/hco/13/GRCh38#53934341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81249650-C-A

53934341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249650-C-T

53934713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81249989-C-T

53934764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250046-T-A

53934812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250093-A-G

53935022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250310-A-G

53935033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250321-G-A

53935097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250398-T-C

53935098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250399-G-A

53935424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250463-C-T

53935439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250478-G-A

53936901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250844-G-A

53937054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81250997-T-G

53938145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251953-T-C