106568243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8740611-G-A

106568243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8740611-G-T

106573537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8742436-G-T

http://identifiers.org/hco/13/GRCh38#106573657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8742553-A-C

http://identifiers.org/hco/13/GRCh38#106573804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8742865-C-A

106573938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8742992-G-A

106573981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8743024-A-G

http://identifiers.org/hco/13/GRCh38#106578913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8746686-C-A

106579124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8746886-G-A

106579551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8747395-G-A

106579665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8747512-G-A

http://identifiers.org/hco/13/GRCh38#106579776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8747622-A-C

106587598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753509-T-G

106587649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753566-A-T

106587775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753707-C-T

106587779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753711-G-T

106588086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753979-G-A

106588086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753979-G-T

106588189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754094-A-G

106588397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754288-A-T

106588443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754339-A-T

106614613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774520-T-C

106614630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774537-G-A

106614630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774537-G-C

106614834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774758-A-G

106619410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783216-C-T

106619424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783231-A-G

106619479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783286-G-A

106619479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783286-G-T

http://identifiers.org/hco/13/GRCh38#106619486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8783293-C-A

http://identifiers.org/hco/13/GRCh38#106619526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8783314-A-C

106619546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783333-T-C

106619620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783401-G-T

106619640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783421-G-A

106619640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783421-G-T

106619909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783857-C-T

106620080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783972-C-G

106620080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783972-C-T

106620365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784160-T-C

106620588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784334-T-C

106620633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784379-G-A

106620905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784576-G-A

106620933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784602-G-T

106620950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784622-G-C

106620995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784668-T-C

106621060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784727-C-T

106621286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8784916-C-T

106621376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8784990-C-T

106621424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785011-A-T

106621556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785145-G-A

106621558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785147-T-A

106621608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785195-A-G

106621701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785305-A-G

106622248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8785826-C-G

106622346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8785924-G-T

106622442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786018-T-C

106622515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786090-G-A

106622548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786111-C-T

106622612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786165-A-G

106622685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786237-C-G

106622833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786387-G-C

http://identifiers.org/hco/13/GRCh38#106622883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8786437-A-C

106622911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786465-T-C

106623218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786762-A-G

106623511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8787052-G-A

106623575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8787114-G-A

106624341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8787797-T-C

106624394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8787832-G-A

106624429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8787872-G-T

106625602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8790884-T-C

106625602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8790884-T-G

106625693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8790971-A-G

106626385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 8793004-A-G

106626394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793013-G-A

106626394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793013-G-C

106626456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793076-A-G

http://identifiers.org/hco/13/GRCh38#106626628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8793233-C-A

106626676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793275-C-T

106626756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793359-A-G

106626777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793380-G-T

106626825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793425-T-C

106626825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793425-T-G

106626960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793518-T-C

106626999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793554-A-G

106627110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793662-G-A

106627110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8793662-G-T

106627138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793688-A-G

106627138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793688-A-T

106627196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793723-G-A

106627196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793723-G-T

106627200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793727-A-G

http://identifiers.org/hco/13/GRCh38#106627204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8793731-C-A

106627204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793731-C-T

106627205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793732-G-A

106627205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793732-G-T

106629003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8796584-A-G

106629013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8796594-A-T

106629083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8796642-G-A

106629097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8796656-T-C

106629298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797205-G-A

106629467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797372-C-G

106629467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797372-C-T

106629655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798021-T-C

http://identifiers.org/hco/13/GRCh38#106630927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8798318-C-A

106630927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8798318-C-G

106631020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8798409-G-A

http://identifiers.org/hco/13/GRCh38#106631165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8798549-C-A

106631189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8798577-T-C

106631388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8798803-G-T

http://identifiers.org/hco/13/GRCh38#106631437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8798852-C-A

106631555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8798942-T-C

106631922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799249-G-A

106633692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802021-G-A

106633692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802021-G-C

106633871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802162-G-A

106633871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802162-G-C

106634166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802440-G-A

106634387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802663-G-A

106634487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803001-G-A

http://identifiers.org/hco/13/GRCh38#106634599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8803113-C-A

106634650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803161-A-G

106634706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803211-T-G

106634745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803250-T-A

106634813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803312-T-C

106634878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803357-C-T

http://identifiers.org/hco/13/GRCh38#106634947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8803426-C-A

106634947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803426-C-T

106634949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803428-A-T

106635207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803689-G-A

106635217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803699-A-T

106635469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803868-T-C

106635584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8803986-G-T

106635821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804160-A-G

http://identifiers.org/hco/13/GRCh38#106635852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8804200-C-A

106636577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804451-C-G

106636608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804469-A-G

106636640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804500-A-G

106636640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804500-A-T

106636641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804501-T-C

http://identifiers.org/hco/13/GRCh38#106636726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8804578-A-C

106636726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804578-A-G

106637318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804803-T-C

106637469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804916-T-C

106637586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804998-A-G

106637684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805061-T-A

106637684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805061-T-C

http://identifiers.org/hco/13/GRCh38#106637708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8805083-A-C

106637788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805162-T-A

106637811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805187-T-C

106637867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805228-T-C

106637875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805236-C-G

106637968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805328-T-C

106638142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805483-G-A

106638437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805768-A-G

106638454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805786-G-A

106638836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806305-G-A

106642156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808081-T-C

106642168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808091-G-A

106642336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808264-C-T

http://identifiers.org/hco/13/GRCh38#106642390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8808320-A-C

106642595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808514-C-T

106642645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808562-A-G

106643449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8811409-A-G

106643678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8811886-T-C

106643785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8812099-G-A

106644282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8812586-T-G

http://identifiers.org/hco/13/GRCh38#106644345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8812649-A-C

http://identifiers.org/hco/13/GRCh38#106644505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8812798-A-C

106644592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8812880-A-G

106644635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8812923-T-A

106645623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816294-T-A

106645624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816295-G-A

106645631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816303-G-A

106645997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816621-T-G

106646076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816701-T-C

106646340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816939-T-G

106646397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816996-C-T

106646398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8816997-T-C

106646418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817017-G-C

http://identifiers.org/hco/13/GRCh38#106646436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8817038-A-C

106646513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817076-G-C

106646712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817247-T-A

106646713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817248-G-A

106646737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817272-C-T

106646739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817274-T-C

106646763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817298-T-C

106646785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817320-G-A

106646970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817512-A-G

106647143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8817685-C-G

106647664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818214-T-C

106647712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818270-T-G

106647790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818346-T-A

106648244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818774-C-G

106648244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818774-C-T

106648527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8819404-G-A

106651146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8822139-T-C

106651246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8822240-T-C

106651529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8822516-G-A

106651594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8822581-C-T

106652022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8823248-C-G

106652554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8823712-A-G

106652625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8823768-A-G

106652872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8824014-T-C

106658277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828103-A-G

106658362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828186-G-A

106658635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828434-G-A

106658660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828443-A-G

106658669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828452-A-G

106658705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828491-T-C

106658709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828495-C-T

106658710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828496-G-A

106658722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828508-G-A

106658748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828533-G-A

106658758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828543-T-A

106658948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8828675-C-T

106659248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829544-A-G

106659263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829558-T-C

106659265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829560-C-G

106659265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829560-C-T

106659515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829801-A-G

106659635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829919-G-T

106659676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829959-C-T

106659699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8829983-C-G

106659731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8830015-C-T

106659869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8830152-A-G

106660046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8830824-A-G

106660046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8830824-A-T

106660414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8831183-G-C

http://identifiers.org/hco/13/GRCh38#106660444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8831211-C-A

106660708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8831618-T-C

106660729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8831635-T-C

http://identifiers.org/hco/13/GRCh38#106660760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8831666-A-C

106661147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8831977-T-C

106661284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832092-C-G

106661329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832136-T-A

106661374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832182-G-A

106661412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832216-C-T

106661668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832462-T-C

http://identifiers.org/hco/13/GRCh38#106661675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8832469-C-A

http://identifiers.org/hco/13/GRCh38#106661703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8832496-A-C

106661740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832538-T-C

106662001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832794-A-G

http://identifiers.org/hco/13/GRCh38#106662047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8832849-A-C

106662110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832892-C-G

106662231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833041-A-G

106662350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833159-A-G

106662442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833264-A-G

106662512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833308-A-G

106662577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833382-C-T

http://identifiers.org/hco/13/GRCh38#106662609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8833412-A-C

106662699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833495-C-G

http://identifiers.org/hco/13/GRCh38#106662736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8833531-C-A

http://identifiers.org/hco/13/GRCh38#106664387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8834791-A-C

106664387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8834791-A-G

106664422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8834829-C-T

http://identifiers.org/hco/13/GRCh38#106664696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8835088-A-C

106664696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835088-A-T

106664821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835221-A-G

106664857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835248-A-G

106664930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835308-T-A

106664951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835326-C-T

106665012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835531-G-A

106665013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8835532-C-T

106665676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8837683-G-A

106665926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8837913-G-A

106666029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8837996-G-A

106666029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8837996-G-T

106666056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8838023-T-C

106666375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8838267-T-C

106667926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8839368-A-G

106667968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8839408-A-G

106668331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8839726-C-T

106668365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8839759-A-G

106668452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8839850-T-C

http://identifiers.org/hco/13/GRCh38#106668511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8839884-C-A

http://identifiers.org/hco/13/GRCh38#106668692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8840029-C-A

106668703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8840039-G-T

106668931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8840226-G-A

106669037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8840338-A-G

106669108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8840452-T-A

106669129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8840472-A-G

106669333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8840743-T-C

106669376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8840836-T-C

106669427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8840883-C-T

106669457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8840913-A-T

106669725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841133-T-C

106669946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841345-C-T

106670045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841445-T-C

106670169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841561-T-C

106670204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841596-C-T

106670398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8841782-T-A

106670654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842033-G-C

106670684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842063-T-C

106670787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842168-A-G

106670948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842419-A-G

106671152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842692-C-G

106671152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8842692-C-T

106671606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843107-G-A

106671611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843109-G-A

106671671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843168-C-T

http://identifiers.org/hco/13/GRCh38#106671723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8843191-C-A

106671772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843235-G-A

106671850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843311-T-C

106671899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843361-G-C

106671922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843384-G-A

http://identifiers.org/hco/13/GRCh38#106672031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8843457-C-A

106672089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843514-A-G

106672112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8843537-T-C

http://identifiers.org/hco/13/GRCh38#106674537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8844243-C-A

http://identifiers.org/hco/13/GRCh38#106674732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8844434-A-C

106674857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8844553-C-G

106678113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846427-T-A

106678207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846505-C-T

106678208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846506-C-T

106678245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846538-A-G

106678380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846682-T-C

106678507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846804-G-A

http://identifiers.org/hco/13/GRCh38#106678621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8846934-A-C

106678892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847188-G-A

106679070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847362-T-C

106679344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847625-G-A

106679344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847625-G-T

106679346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847627-A-G

106679419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847693-G-A

106679419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847693-G-T

106679468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8847742-G-T

http://identifiers.org/hco/13/GRCh38#106679573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8847834-C-A

106680408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851238-C-G

106680482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851312-G-C

106680508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851329-C-T

106680617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851457-C-T

106680641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851483-G-A

106681109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8851958-T-C

106681239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852063-T-G

106681406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852209-C-T

106681408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852211-T-C

http://identifiers.org/hco/13/GRCh38#106681414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8852217-C-A

106681424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852227-C-G

106681497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852320-G-A

106681548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852371-T-G

http://identifiers.org/hco/13/GRCh38#106681567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8852390-A-C

106681567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852390-A-G

106682056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852856-A-T

106682057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8852857-T-A

106682316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853145-C-T

106682389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853225-A-G

106682389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853225-A-T

106682482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853299-G-T

106682729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853581-A-G

106682762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853603-C-G

106682799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853638-C-T

http://identifiers.org/hco/13/GRCh38#106682902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8853770-C-A

http://identifiers.org/hco/13/GRCh38#106683320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#8853879-C-A

106683320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8853879-C-G

106683320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8853879-C-T

106683323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8853882-T-C

106683368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8853928-G-A

106683480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854013-C-T

106683532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854061-G-A

106683532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854061-G-C

106683597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854113-A-G

106683719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854213-T-C

106683782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854279-C-T

106683806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854311-G-T

106683891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854403-T-C

106683892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854404-C-T

106683935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8854444-G-A

http://identifiers.org/hco/13/GRCh38#106684092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8854603-C-A

http://identifiers.org/hco/13/GRCh38#106684188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8854695-A-C

106684750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8855422-T-C

106684912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8855573-A-G

106685083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8855721-C-T

106685290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8855907-C-T

106685326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8856016-A-G

106685338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8856030-G-A

106685338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8856030-G-C

106685436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8856395-C-T

106685460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8856418-C-T

106685908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8856874-T-C

106686204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8857187-G-A

106691004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8859672-G-C

106691533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860150-C-T

106691583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860198-C-T

106691743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860358-T-C

106691806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860421-A-G

106691847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860462-C-G

106691885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860512-C-T

106691948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860576-C-T

106691949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860577-A-T

http://identifiers.org/hco/13/GRCh38#106691950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8860578-C-A

106691950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860578-C-G

106691950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860578-C-T

http://identifiers.org/hco/13/GRCh38#106692030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8860658-A-C

106692044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860672-C-T

106692100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860728-T-A

http://identifiers.org/hco/13/GRCh38#106692142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8860754-C-A

106692142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860754-C-G

106692200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8860813-T-C

http://identifiers.org/hco/13/GRCh38#106692266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8860853-C-A

106692452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8861035-T-C

106692587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8861208-C-T

106692826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8861436-C-T

106695478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8862635-T-A

106695668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8862813-G-A

106695696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8862841-A-G

106695796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8862936-T-A

106695982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863102-A-G

106695990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863106-T-C

106696184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863655-A-T

106696276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863760-A-G

http://identifiers.org/hco/13/GRCh38#106696407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8863892-C-A

106696460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863944-G-A

106696460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8863944-G-T

106696529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864010-C-T

http://identifiers.org/hco/13/GRCh38#106696564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8864044-C-A

106696564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864044-C-T

106696630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864106-C-T

106696932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864324-T-C

106696945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864336-A-T

http://identifiers.org/hco/13/GRCh38#106697041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8864425-C-A

106697073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864457-A-G

http://identifiers.org/hco/13/GRCh38#106697196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8864570-C-A

106697196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864570-C-G

106697196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8864570-C-T

106697397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8864770-A-G

106697727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8865101-A-G

106697915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8865231-G-A

106697915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8865231-G-T

http://identifiers.org/hco/13/GRCh38#106697943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8865257-C-A

106699252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8866255-G-A

106699268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8866271-C-T

106699403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8866382-T-A

106699569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867376-T-A

106699699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867507-T-C

106699764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867566-G-C

106699788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867575-C-T

106699811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867597-T-C

106699985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867764-A-G

106700044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8867823-A-G

106700243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868021-G-A

106700369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868112-T-C

106700412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868153-T-A

106700590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868332-A-G

106700610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868351-A-G

106700744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868477-C-T

106700998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868634-G-A

106701011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868637-C-T

106701404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8868932-G-A

106701647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8869161-G-T

http://identifiers.org/hco/13/GRCh38#106701714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8869211-C-A

106701742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8869239-G-A

106702311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8869811-C-T

http://identifiers.org/hco/13/GRCh38#106702344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8869844-C-A

106702344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8869844-C-G

106702865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8870794-G-A

106702879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8870807-T-C

106702885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8870813-A-G

106703036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8870965-A-G

106703101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871029-A-G

106703164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871091-T-A

106703193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871121-G-C

106703367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871261-T-C

106703451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871340-T-A

106703451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871340-T-C

106703573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871456-G-A

106703735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871647-A-G

106703735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871647-A-T

106703839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871724-T-G

106703908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871790-C-T

106704031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871905-T-C

106704031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8871905-T-G

106704692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8872661-G-T

106704735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8872703-G-A

106705080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8872979-T-G

106705279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8873175-A-G

106705402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8873290-G-A

106705430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8873317-T-C

106705736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8873589-A-G

106705903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8873752-T-C

106706169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874015-T-C

106706506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874269-C-T

106706531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874317-G-T

http://identifiers.org/hco/13/GRCh38#106706907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8874822-C-A

106706907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874822-C-T

106706916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874831-G-C

106706916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874831-G-T

106707012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874941-G-A

106707012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8874941-G-C

http://identifiers.org/hco/13/GRCh38#106707818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8875173-C-A

106708418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8875762-T-G

106708522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8875865-G-T

106708547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8875890-C-T

106708728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876059-C-G

http://identifiers.org/hco/13/GRCh38#106708908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8876250-C-A

106709169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876482-T-C

106709362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876619-A-G

106709424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876685-A-T

106709585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876825-G-A

106709774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8876976-C-T

106709808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877010-G-A

106709808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877010-G-T

106709850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877051-C-G

106709884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877086-A-G

106710034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877233-G-T

106710389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877578-A-G

106710389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877578-A-T

106710614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877802-T-C

106710704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8877890-T-C

106711257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878319-G-A

106711271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878333-G-A

106711272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878334-T-C

http://identifiers.org/hco/13/GRCh38#106711292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8878353-A-C

106711292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878353-A-G

106711310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878371-G-A

http://identifiers.org/hco/13/GRCh38#106711583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8878566-C-A

106711644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878580-C-T

106712100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8878943-T-G

106712255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879119-G-A

http://identifiers.org/hco/13/GRCh38#106712280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8879144-A-C

106712280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879144-A-G

106712325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879186-T-C

106712455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879344-T-C

106712777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879651-C-T

106712912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879790-G-A

106713091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879960-C-T

106713108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8879975-G-A

106713169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880032-T-C

106713229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880085-T-A

106713282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880139-A-G

106713545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880508-C-T

106713546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880509-A-G

106713564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8880528-G-A

106714399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881425-G-A

106714428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881469-G-T

106714429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881470-T-C

http://identifiers.org/hco/13/GRCh38#106714431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8881472-C-A

106714435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881476-C-T

106714489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881529-C-G

106714489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881529-C-T

106714494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881534-C-G

106714617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881647-C-G

106714850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881843-A-G

106714917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8881893-G-A

106715049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882171-T-C

106715059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882203-C-G

106715067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882211-C-T

http://identifiers.org/hco/13/GRCh38#106715186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8882323-C-A

106715186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882323-C-T

106715269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882405-A-G

106715426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882560-T-A

106715470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43691
most severe consequence: non coding transcript exon variant
orthologous variants: 8882604-C-T