91985176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96592013-A-G

91985199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591992-G-A

91985199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591992-G-T

91985274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591918-A-G

91985274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591918-A-T

91985436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591755-G-T

91985464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591722-G-T

91985465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591721-G-T

http://identifiers.org/hco/12/GRCh38#91985483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96591703-C-A

91985571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591619-C-G

91985768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591427-C-T

91985851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591345-A-G

http://identifiers.org/hco/12/GRCh38#91985876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96591321-C-A

91985876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591321-C-T

91985945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96591252-A-G

91986261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96590940-T-C

91986308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96590783-T-C

http://identifiers.org/hco/12/GRCh38#91986373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#96590625-C-A

91986373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96590625-C-T

http://identifiers.org/hco/12/GRCh38#91986465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96590534-C-A

91986465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96590534-C-T

http://identifiers.org/hco/12/GRCh38#91986468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96590531-C-A

91986468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96590531-C-T

91986553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96590474-G-T

91986720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96590314-A-T

http://identifiers.org/hco/12/GRCh38#91986764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96590272-C-A

91986772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96590264-T-A

91986772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96590264-T-C

http://identifiers.org/hco/12/GRCh38#91987592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96590127-C-A

91987592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96590127-C-G

91987640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96590084-A-G

http://identifiers.org/hco/12/GRCh38#91987771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96589946-A-C

91988067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96589886-G-A

91988115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96589839-T-C

http://identifiers.org/hco/12/GRCh38#91988292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96589679-C-A

91988504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96589446-G-C

http://identifiers.org/hco/12/GRCh38#91988660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96589162-C-A

91988981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96588844-T-G

91989121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non coding transcript exon variant
orthologous variants: 96588732-G-C

http://identifiers.org/hco/12/GRCh38#91989370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96588537-C-A

91989370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96588537-C-T

91989486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96588432-G-A

91990293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96588116-G-A

http://identifiers.org/hco/12/GRCh38#91990294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96588115-C-A

91990347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96588065-T-C

91990347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96588065-T-G

http://identifiers.org/hco/12/GRCh38#91990375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96588037-C-A

91990384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96588028-T-A

91990449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587989-A-G

91990628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587811-G-T

91990681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587758-T-C

91990831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587622-C-T

91990843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587610-T-C

http://identifiers.org/hco/12/GRCh38#91990963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96587457-A-C

91991054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587357-T-C

91991180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587251-A-G

91991291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96587134-C-T

91991629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586821-T-C

91991634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586812-T-G

91991771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586725-C-T

91992033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586478-C-T

91992046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586465-C-T

91992173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586340-C-T

91992348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586192-T-A

91992348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586192-T-C

91992349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96586191-T-C

91992619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585721-T-A

http://identifiers.org/hco/12/GRCh38#91992650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96585572-C-A

91992678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585545-A-G

91992835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585393-G-A

91992835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585393-G-C

91993026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585202-T-C

91993077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96585155-G-C

91993202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96585044-T-C

91993230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96585013-A-G

91993338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96584835-C-T

http://identifiers.org/hco/12/GRCh38#91993637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96584256-C-A

91993637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96584256-C-G

91993637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96584256-C-T

91993771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96584126-G-A

http://identifiers.org/hco/12/GRCh38#91994099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96583807-A-C

http://identifiers.org/hco/12/GRCh38#91994263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96583647-A-C

http://identifiers.org/hco/12/GRCh38#91994377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96583533-A-C

91994931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96582976-A-G

91995022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96582901-A-G

92002256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96581127-G-C

92002298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96581076-T-A

92002298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96581076-T-C

92002436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580965-G-A

92002597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580815-C-G

92002662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580774-T-A

92002720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580714-T-G

92002737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580699-C-T

92002929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96580499-T-C

92003484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96579950-T-C

http://identifiers.org/hco/12/GRCh38#92004345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96578882-A-C

92005154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96578369-A-G

92005356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96578182-T-C

http://identifiers.org/hco/12/GRCh38#92005360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96578178-C-A

92006059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96577865-T-C

92006110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96577812-T-G

92006405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96577538-A-G

92006424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96577519-G-T

92008798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576772-T-C

92008886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576677-G-A

92009234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576266-G-A

92009234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576266-G-C

http://identifiers.org/hco/12/GRCh38#92009244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96576256-C-A

92009244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576256-C-T

92009432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96576065-A-G

92009630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575857-A-G

92009631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575856-G-A

92009671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575824-C-T

92009713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575783-T-C

92009756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575724-T-C

92009789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575691-G-C

92009865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575619-G-A

92009924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575554-G-T

92010013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575461-G-A

92010013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575461-G-C

92010169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575347-G-A

92010218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96575297-A-G

92010612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96574908-G-A

92011365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96574435-G-A

92011365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96574435-G-C

92011675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96574266-T-A

http://identifiers.org/hco/12/GRCh38#92012014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96574007-A-C

92012626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573707-T-C

92012645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573690-C-T

92012720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573614-A-G

92012804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573530-A-G

92018829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573235-C-G

92018899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573157-G-T

92018913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573143-A-G

92018955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573119-A-G

92019005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96573069-A-G

92019354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96572713-A-T

92019612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96572165-G-C

92019724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96572031-A-G

92019807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571948-C-T

92019858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571892-C-G

92019865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571885-A-G

92020055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571676-C-G

92020207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571538-T-A

http://identifiers.org/hco/12/GRCh38#92020308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96571377-C-A

92020409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571276-T-G

92020460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571220-T-C

92020612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96571064-C-T

92020661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96571018-C-T

92020662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96571017-T-C

92020711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570978-T-C

92020736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570952-A-T

92020746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570942-T-C

92020833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570854-T-A

92020904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570781-C-T

92021032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570201-T-C

92021065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570173-C-G

92021379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96570027-G-A

92021479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569925-G-A

92021483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569921-G-T

92021689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569713-A-T

92021817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569568-T-C

92021825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569560-C-T

92021844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569541-C-T

92021866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569519-A-G

92022047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569341-G-A

92022163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96569254-T-C

92022498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96568933-G-T

92022499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96568932-C-T

92022511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96568920-T-G

92025388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96567142-T-C

92025434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96567093-T-A

92025434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96567093-T-C

92025521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566996-A-G

92025561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566956-T-C

92025663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96566863-T-A

92025687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566839-A-G

92026146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566414-A-G

http://identifiers.org/hco/12/GRCh38#92026211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96566350-C-A

92026247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566315-T-C

92026336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96566253-A-G

92026488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96566147-A-G

92028185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96563534-G-A

92028185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96563534-G-T

92028242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96563477-A-G

92028460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96563264-C-T

92028621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96563101-G-A

92028621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96563101-G-T

http://identifiers.org/hco/12/GRCh38#92028915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96562540-C-A

92028935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96562520-C-T

http://identifiers.org/hco/12/GRCh38#92028992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96562463-C-A

92029070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96562388-A-G

92029212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96562258-A-G

92029399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96562076-T-C

92030180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96561506-T-C

92030181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96561505-G-T

92030234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96561453-G-A

92030466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96561211-A-G

92030979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96560757-A-G

92032206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96560571-G-A

92032274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96560506-G-A

92032465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96560057-G-A

92032601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96559918-T-C

92033267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96559347-A-G

92033540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96559124-T-C

92034853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558703-A-G

92034984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558576-T-G

92035093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558466-G-A

92035093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558466-G-T

92035106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558453-A-G

92035111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558448-G-C

92035285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558276-C-G

92035497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96558099-G-T

92036163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96557316-T-A

92036163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96557316-T-C

92036465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96557004-T-C

92036900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96556506-T-A

92037150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96556257-C-T

92037340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96556097-C-T

92037459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96555980-C-T

http://identifiers.org/hco/12/GRCh38#92038160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96554560-C-A

92038541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96554225-C-T

92038542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96554224-G-A

92038610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96554164-A-G

92038611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96554163-G-C

92038738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96554044-G-A

92038947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96553846-T-G

92039274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96553226-C-G

http://identifiers.org/hco/12/GRCh38#92039508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96552981-C-A

92039594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96552669-T-C

92039616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96552647-T-C

92039734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96552186-C-T

92039858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96552065-T-C

http://identifiers.org/hco/12/GRCh38#92039963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96551963-C-A

92041048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96550818-A-T

92041284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96550591-T-G

92042254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96548071-G-A

92042280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96548045-C-T

92045998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96546474-T-C

92047434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96544743-G-A

92047496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96544663-G-C

92047995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96544194-A-G

92048638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96543586-A-T

92048747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96543515-G-C

92048793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96543447-C-T

92048871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96543357-G-T

92048994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96543206-G-A

92049395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96542922-A-T

http://identifiers.org/hco/12/GRCh38#92049649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96542701-C-A

92049706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96542648-T-C

92049723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96542630-C-T

92049927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96542430-G-C

92049928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96542429-G-A

92050539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96541386-A-G

92054058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537982-T-G

http://identifiers.org/hco/12/GRCh38#92054207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96537823-C-A

92054207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537823-C-T

http://identifiers.org/hco/12/GRCh38#92054309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96537734-C-A

92054536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537524-G-A

92054944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537425-T-C

92055161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537215-A-G

92055319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96537022-A-T

92055441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536907-G-A

92055892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536634-A-G

92055901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536625-G-T

92055975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536548-T-C

92056135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96536385-A-G

92056136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96536384-C-T

92056251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536269-G-A

92056352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536148-G-A

92056482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96536020-A-G

92056590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96535919-A-G

92058214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96535884-G-A

92058415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96535695-G-A

92059484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96534221-G-A

92060059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96533688-G-A

92060059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96533688-G-T

http://identifiers.org/hco/12/GRCh38#92060187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#96533560-A-C

92060235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96533499-A-G

92060303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96533430-T-C

http://identifiers.org/hco/12/GRCh38#92060801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96533001-C-A

92060872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96532931-G-T

92061054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96532778-T-C

92061326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96532503-C-G

92061769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96532061-G-T

92062160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96532011-C-T

92063072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96529922-T-C

92063214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96529777-G-A

92064086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96528852-T-C

92064419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96527895-G-T

92064448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96527868-C-T

92065307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96526933-G-A

92065761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96526499-G-T

92066507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96525942-C-T

http://identifiers.org/hco/12/GRCh38#92068661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96525369-C-A

92068681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96525347-A-G

92069045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96524976-G-C

92069046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96524973-G-A

92069246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96524811-A-G

92069298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96524739-C-T

92069551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96523787-G-A

92069674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96523670-G-C

92069686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96523658-G-T

92069748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96523594-T-C

92069831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96523514-G-T

92071101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96522316-A-G

92071174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96522226-C-T

92071207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96522193-C-T

http://identifiers.org/hco/12/GRCh38#92071359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96522042-A-C

92071449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521955-A-G

92071594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521758-A-G

92071642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521711-G-A

92072080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521580-G-A

92072080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521580-G-C

92072080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96521580-G-T

92072775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96520956-T-C

92073467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96520392-T-C

92074823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96520055-A-G

92075572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96518278-C-T

92075845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96518024-G-A

92077025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517440-C-T

92077026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517439-A-G

92077180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517292-G-A

92077243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517233-C-T

92077293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517181-C-T

92077307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96517167-A-G

92077689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96516806-T-G

92077754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96516765-G-A

92077992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96516347-A-T

92078302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96516113-T-C

92078404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96516041-C-T

92078605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96515824-G-A

92078617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96515812-G-C

92078824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96515560-T-C

92079028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96515196-G-C

92079105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96515132-T-G

92079530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96514189-T-G

92080464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96513472-G-A

92080633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96513331-A-G

92080671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96513295-A-G

92081913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96513036-A-G

92082179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512782-G-C

92082355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512617-A-G

92082389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512583-T-C

92082453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512420-G-A

92082528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512356-T-C

92082678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512225-A-G

92082684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512219-T-C

92082707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512196-A-G

92082855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96512073-G-T

92083844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96510633-T-C

92083926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96510550-C-T

92084961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96503521-T-A

92085115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96503450-C-T

92085462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96502574-A-G

92085638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96502414-A-G

http://identifiers.org/hco/12/GRCh38#92085816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96502232-C-A

92086169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96501910-A-G

92086383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96501587-A-G

92086394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96501572-T-C

92086568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96500985-C-T

http://identifiers.org/hco/12/GRCh38#92086774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96500775-C-A

http://identifiers.org/hco/12/GRCh38#92086862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96500682-A-C

92086862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96500682-A-G

92087505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96500341-C-T

http://identifiers.org/hco/12/GRCh38#92088115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96499791-A-C

92088117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96499789-C-T

92088212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96499756-G-T

http://identifiers.org/hco/12/GRCh38#92088703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96499442-A-C

92088782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96499371-G-T

92089034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498972-G-A

92089041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498963-G-C

92089047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498957-G-A

92089117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498882-A-G

92089353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498530-T-A

92089362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498521-T-C

92089393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498455-A-G

92089626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498154-C-G

92089698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498074-C-T

92089701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498071-G-T

92089717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96498056-A-G

92090628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96497222-C-T

92090655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96497195-C-T

92090880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96496967-A-T

92090939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96496871-T-C

92091129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96496637-A-G

92092097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96495181-G-A

92092279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96494993-T-C

92094873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96493002-T-C

92094912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492964-T-A

92095175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492713-A-G

92095615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492227-G-A

92095634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492204-T-G

92096000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492148-C-T

92096142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492005-C-G

92096142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96492005-C-T

92096542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96491271-T-G

92098135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490965-A-G

92098240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490846-C-T

92098572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490714-C-G

92098657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490605-T-C

http://identifiers.org/hco/12/GRCh38#92098841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96490449-C-A

92099010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490266-G-A

92099166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490202-G-A

92099317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490058-A-G

92099317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490058-A-T

92099327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490048-G-A

92099353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96490030-T-C

92099515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489901-G-A

92099548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489867-T-C

92099784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489595-G-A

http://identifiers.org/hco/12/GRCh38#92099969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96489415-C-A

92099997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489385-G-A

92099999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489383-G-A

http://identifiers.org/hco/12/GRCh38#92100451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96489327-A-C

http://identifiers.org/hco/12/GRCh38#92100583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96489199-C-A

92100583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489199-C-T

92100748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96489029-A-G

92101597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96488834-C-G

92102120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96488242-A-G

92105859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96484708-G-A

92105977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96484328-A-G

92106046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96484249-T-C

92106152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96484142-G-C

92106152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96484142-G-T

92106347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96483919-C-T

92106404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96483864-G-A

92106447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96483803-C-G

92106492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96483773-C-G

92106492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96483773-C-T

92107442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96482730-G-T

http://identifiers.org/hco/12/GRCh38#92107527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96482628-A-C

http://identifiers.org/hco/12/GRCh38#92107637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96482514-C-A

92107637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96482514-C-T

92108091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96482080-A-G

92108527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96481666-C-T

92108593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96481574-T-C

92108606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96481561-G-T

http://identifiers.org/hco/12/GRCh38#92108681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96481478-C-A

92108875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96481256-G-C

92108955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96481177-T-C

92110355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96480637-T-A

92110383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96480609-C-G

92110383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96480609-C-T

92111336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478933-A-G

92111371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478904-C-T

92111391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478884-T-A

92111451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478824-A-G

92111581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478706-C-T

92111746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478547-C-T

92111966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96478365-T-C

92122316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96477093-T-A

92123236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96475621-C-T

92123448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96475397-T-C

92124119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96474655-A-G

92124296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96474501-T-C

92124407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96474351-T-G

92124888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473647-C-T

92124904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473630-G-A

http://identifiers.org/hco/12/GRCh38#92125253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96473462-C-A

92125523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473330-T-C

92125553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473304-A-T

92125660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473163-A-G

92125753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96473091-G-A

92125955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472896-C-T

92126423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472227-T-C

92126524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472179-T-A

92126525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472178-A-T

92126565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472147-T-G

92126594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472130-A-G

92126594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472130-A-T

92126600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472124-C-T

92126603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472121-G-A

92126603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96472121-G-T

92126749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471975-G-A

http://identifiers.org/hco/12/GRCh38#92126750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96471974-A-C

92126750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471974-A-G

92126751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471973-C-T

92126807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471932-A-T

92126991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471746-G-A

92127077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471665-C-T

92127176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471544-T-C

92127208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96471459-C-T

92131167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96470255-T-C

http://identifiers.org/hco/12/GRCh38#92131229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96470195-C-A

92131389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96470050-G-A

92131513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469930-C-T

92131605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469856-A-T

92131779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469681-G-T

92131874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469587-G-A

92131874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469587-G-T

92132298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96469035-C-T

92132354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96468981-T-C

92132608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467782-A-G

92132777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467624-T-A

92132920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467543-C-T

92133025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467438-G-T

http://identifiers.org/hco/12/GRCh38#92133364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96467125-C-A

92133364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467125-C-G

92133431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96467067-G-T

92134354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96465245-A-G

92134361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96465236-T-C

92134462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96465130-A-G

92134555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96465084-G-A

92134640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96465008-A-G

92135147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96464295-C-T

92135279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96464166-A-G

92135302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96464142-T-C

92135738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96463635-G-A

92135738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96463635-G-T

http://identifiers.org/hco/12/GRCh38#92136022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96463170-C-A

92136022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96463170-C-T

http://identifiers.org/hco/12/GRCh38#92136059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96463136-A-C

92136086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96463094-C-T

92136230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96462949-G-C

92136305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96462882-A-G

92136521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96462740-C-T

92136571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96462693-C-T

92136683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96462592-C-G

92137317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96461824-C-G

92137418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96461717-T-C

92137996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96461185-A-G

92138123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460806-T-C

http://identifiers.org/hco/12/GRCh38#92138258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96460668-A-C

http://identifiers.org/hco/12/GRCh38#92138324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96460615-A-C

92138528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460428-A-G

92138556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460401-C-T

92138571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460386-T-C

92138666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460311-T-C

92138738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460239-C-T

92138753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460224-G-A

92138810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96460165-A-T

http://identifiers.org/hco/12/GRCh38#92138811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#96460164-A-C

92139229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96459822-T-C

92139469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96459480-T-C

92140222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96458788-T-C

92140459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96458489-A-G

92140463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96458485-A-G

92140785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96458196-A-G

92140785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96458196-A-T

92141043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96457998-T-C

92141424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96457490-G-A

http://identifiers.org/hco/12/GRCh38#92141621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#96457119-C-A

92141672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96457069-A-T

http://identifiers.org/hco/12/GRCh38#92141775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#96456993-C-A

92141775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456993-C-T

92141782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456986-T-A

92141900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456879-A-T

92142026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456725-G-A

92142026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456725-G-T

92142067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456688-A-G

92142135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456463-T-C

92142163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456432-A-G

92142197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456388-G-C

92142212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456373-G-T

92142461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456092-A-G

92142461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456092-A-T

92142489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456062-C-G

92142551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96456030-G-T

http://identifiers.org/hco/12/GRCh38#92142805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#96455786-A-C

92142805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27409
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96455786-A-G