105177900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5190698-C-T

http://identifiers.org/hco/11/GRCh38#105177930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#5190668-C-A

105178022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5190573-A-G

105178189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190454-T-G

105178651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190311-G-C

105178668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190294-T-C

105178670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190292-T-C

105178766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190234-T-C

105178837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190178-A-G

105178868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190143-C-T

105178948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190065-T-C

105179080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189750-T-A

105179138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189694-T-C

http://identifiers.org/hco/11/GRCh38#105179161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5189671-C-A

105179256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189576-G-T

105179276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189564-T-C

105179304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189527-A-G

105179652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189187-A-G

105179770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189112-A-G

105179836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189043-A-T

105179844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189035-G-A

105179844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189035-G-C

105179844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189035-G-T

105179999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188885-G-C

105180142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188743-C-T

105180260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188629-C-G

105180260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188629-C-T

105181096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187101-T-A

105181198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187011-C-T

105181225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186984-T-G

105181384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186832-C-G

105181384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186832-C-T

105181518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186710-A-G

105181635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186616-A-G

105181799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5186544-C-G

105181872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5186461-C-T

105221784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5166333-T-C

105221840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5166289-G-T

105221841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5166288-C-T

105222180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165944-G-A

105222229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165901-T-C

105222271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165859-T-C

105222813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165270-T-C

105223141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165188-T-C

105223159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165170-T-C

http://identifiers.org/hco/11/GRCh38#105223420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5164952-C-A

105223420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164952-C-T

105223463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164907-C-T

105223557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164808-T-C

105223631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164734-A-T

105223884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164483-A-G

105225192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164156-G-C

105225314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163894-T-G

105225512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163679-A-G

105225567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163627-T-C

105225709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163517-C-T

105225819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163412-C-T

105225851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163380-A-G

105225920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163307-T-C

105226030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163224-T-A

105226062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163200-G-A

105226074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163194-G-T

105226229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163045-T-C

105226557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5162750-T-A

105226611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5162696-G-T

105226795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5162489-A-G

http://identifiers.org/hco/11/GRCh38#105232843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5156113-A-C

105233167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5155923-C-T

105233239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5155847-G-A

http://identifiers.org/hco/11/GRCh38#105267648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5123665-C-A

105267678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5123634-A-G

105267703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5123616-G-T

105268041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5123320-T-G

105268127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5123224-T-C

http://identifiers.org/hco/11/GRCh38#105268175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5123176-C-A

105273629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5120128-T-C

105273675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5120083-G-C

105273677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5120081-C-T

http://identifiers.org/hco/11/GRCh38#105273840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5119911-C-A

105273878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119873-A-G

105273881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119870-T-C

105273895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119856-T-C

http://identifiers.org/hco/11/GRCh38#105273923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5119770-A-C

105273936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119751-A-G

105274117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119579-A-G

105274396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119337-A-G

105274655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5119116-T-A

105274874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5118854-T-C

105274895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5118835-T-A

105274895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5118835-T-C

105275075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5118707-G-C

105275140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5118641-T-C

105282791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113255-T-C

http://identifiers.org/hco/11/GRCh38#105282944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5113414-C-A

105282981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113445-C-T

105283016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113475-G-A

105283041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113499-C-T

105283073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113535-T-C

105283114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113558-T-C

105283115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113559-C-T

http://identifiers.org/hco/11/GRCh38#105283258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5113676-C-A

105283258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113676-C-G

105283517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113924-A-T

105283566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5113966-G-A

105297646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5110950-T-C

105297646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5110950-T-G

105298659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5109335-C-T

105298674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5109319-C-T

105298712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5109275-T-A

105298785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5109203-A-G

105299307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5108306-T-C

105339587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053645-T-A

http://identifiers.org/hco/11/GRCh38#105339606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5053626-A-C

105339617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053614-G-A

105339721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053510-G-T

105339906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053326-T-C

105339980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053274-G-C

105339980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053274-G-T

105339981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053273-G-T

105340056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5053226-G-T

105340345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052919-T-G

105340438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052293-A-G

105340586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052164-A-G

105340674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052098-T-C

105355529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047153-G-T

http://identifiers.org/hco/11/GRCh38#105355739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5046944-C-A

105356020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045624-A-G

105356063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045576-C-T

105364119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044842-C-T

105364145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044812-T-A

105364145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044812-T-C

105364171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044779-C-G

105364171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044779-C-T

http://identifiers.org/hco/11/GRCh38#105364239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5044710-C-A

105364244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044705-C-T

105364290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044660-A-T

105364348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044617-T-C

105364351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044614-A-T

105364405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044561-G-T

105364425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044542-G-A

105364624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044346-T-C

105364706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044255-C-G

105364921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044096-G-A

105365814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043822-T-C

105366116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043524-T-C

105366153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043496-G-T

105366193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043456-G-T

105372350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5039134-T-A

105372350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5039134-T-C

105372467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5039015-A-G

105373735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5038196-T-C

105374303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035012-C-T

105374324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034991-G-A

105374324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034991-G-C

105374324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034991-G-T

105403192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5026078-C-T

105403361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025902-A-G

105403482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025781-G-A

105403592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025674-A-G

105403704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025578-G-C

105403723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025559-C-T

105403780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025506-A-G

105403781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025505-C-T

105403812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025485-T-C

105404904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022123-T-C

http://identifiers.org/hco/11/GRCh38#105405185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5021857-C-A

105405214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021825-T-C

105405266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021776-G-C

105405384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021671-G-T

105405575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021460-T-A

105405796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020905-C-G

105405801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020900-A-G

105406077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020624-G-A

http://identifiers.org/hco/11/GRCh38#105406081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5020620-A-C

105406150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020554-T-C

105406348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020273-C-T

105407058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019558-G-T

105407074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019546-G-A

105407380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019275-T-C

105407856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018868-G-A

105407969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018784-G-C

105408069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018689-A-G

105408117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018640-G-A

105408306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018461-T-C

105408591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018257-T-C

105408613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5018230-T-C

105408856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5017997-G-A

105409384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5017520-A-T

105409542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5017367-G-C

http://identifiers.org/hco/11/GRCh38#105409952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5017096-A-C

105409952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5017096-A-G

105409998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5017050-G-C

http://identifiers.org/hco/11/GRCh38#105410141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5016911-A-C

105410437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5014288-G-T

105410489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5014240-G-A

105410489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5014240-G-C

105410932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013788-T-G

http://identifiers.org/hco/11/GRCh38#105411072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#5013607-C-A

105411072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013607-C-T

105411318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013374-A-G

105411333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013359-C-T

105411352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013339-G-T

105411472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5013208-G-A

105411946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5012872-T-C

105412124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010585-A-G

105412151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010555-T-G

105424925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4997359-T-C

105425390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4996926-C-T

http://identifiers.org/hco/11/GRCh38#105427733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4996467-C-A

105427896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4996317-G-A

http://identifiers.org/hco/11/GRCh38#105428219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4995932-C-A

105428896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4995567-T-C

105429312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4995164-T-C

105430112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994383-A-G

http://identifiers.org/hco/11/GRCh38#105430284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4994202-A-C

105430358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994129-C-G

105430358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994129-C-T

105454388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4969145-A-G

105454414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4969120-A-T

105454886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968711-C-G

105470767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4952090-T-A

105471052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951811-G-A

105471052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951811-G-C

105471287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951592-A-G

105475196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4940181-A-T

105475375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4939994-G-A

105475430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4939938-T-A

105475430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4939938-T-C

105489566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4936242-T-C

105489623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4936190-T-C

105490336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935334-G-C

105490425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935261-C-T

105490514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935169-A-T

105491097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932936-C-T

http://identifiers.org/hco/11/GRCh38#105491215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932818-C-A

http://identifiers.org/hco/11/GRCh38#105491219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932814-C-A

105491219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932814-C-T

http://identifiers.org/hco/11/GRCh38#105491223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932810-C-A

http://identifiers.org/hco/11/GRCh38#105491227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932806-C-A

http://identifiers.org/hco/11/GRCh38#105491235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932798-C-A

http://identifiers.org/hco/11/GRCh38#105491237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932796-C-A

http://identifiers.org/hco/11/GRCh38#105491243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932790-A-C

http://identifiers.org/hco/11/GRCh38#105491245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932788-A-C

http://identifiers.org/hco/11/GRCh38#105491267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932766-A-C

105491267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932766-A-G

105491291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932742-G-A

105491291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932742-G-T

http://identifiers.org/hco/11/GRCh38#105491298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#4932735-C-A

105491298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932735-C-T

105491510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932498-T-A

105491563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932451-C-G

105491747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28861
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932268-C-T