27919424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111478456-C-T

27919464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478414-A-G

27919464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478414-A-T

http://identifiers.org/hco/22/GRCh38#27919469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111478409-C-A

27919469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478409-C-T

http://identifiers.org/hco/22/GRCh38#27919483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111478398-C-A

27919483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478398-C-G

27919483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478398-C-T

27919518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111478363-G-A

27919518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111478363-G-C

27919535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111478347-T-A

27922336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111477991-T-C

27922387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111477919-G-A

27922588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111477724-A-G

27922674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111477639-T-C

27948288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111452643-C-G

27948312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111452619-A-G

27949324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111451722-A-G

27949640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111451381-C-T

27949687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111451327-T-C

http://identifiers.org/hco/22/GRCh38#27949848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111451173-C-A

27949848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111451173-C-T

27973551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111442579-G-A

27973551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111442579-G-T

27973865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111441869-A-G

27974881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111441072-G-A

27978100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111437563-T-C

27978909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436982-A-G

27979007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436862-G-T

27979162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436723-T-C

http://identifiers.org/hco/22/GRCh38#27979629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111436541-C-A

27979629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436541-C-G

27979629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436541-C-T

http://identifiers.org/hco/22/GRCh38#27979657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111436513-C-A

27979658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436512-T-A

27979772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436414-A-G

http://identifiers.org/hco/22/GRCh38#27979839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111436369-C-A

27979874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436333-A-G

27979891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436316-G-T

27979912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436291-T-C

http://identifiers.org/hco/22/GRCh38#27980005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111436213-A-C

27980005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111436213-A-G

27980257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111435987-G-T

27981237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111435297-T-G

27981448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111435084-A-G

27981634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434879-T-C

27981668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434850-A-G

http://identifiers.org/hco/22/GRCh38#27981729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111434788-C-A

27981729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434788-C-T

27981730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434787-A-G

27981970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434645-G-A

27981970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434645-G-T

http://identifiers.org/hco/22/GRCh38#27981975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111434640-A-C

27981975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434640-A-G

27982089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434542-G-A

27982089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434542-G-T

27982101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434531-C-T

http://identifiers.org/hco/22/GRCh38#27982106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111434526-C-A

27982106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434526-C-T

27982134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434491-T-C

27982144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434476-G-A

27982144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434476-G-T

http://identifiers.org/hco/22/GRCh38#27982145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111434475-C-A

27982145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434475-C-T

27982296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434336-G-A

27982296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434336-G-T

http://identifiers.org/hco/22/GRCh38#27982297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111434335-C-A

27982297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434335-C-T

27982403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434238-C-G

27982403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111434238-C-T

27982708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433963-G-A

27982792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433900-C-T

27982891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433798-A-G

27982891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433798-A-T

27982969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433732-G-A

27983356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433351-C-T

27983368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433339-T-C

27983436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433271-G-A

27983436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433271-G-T

27983437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433270-C-G

27983437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433270-C-T

27983455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433252-T-C

27983455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433252-T-G

27983582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111433125-C-T

27983878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432830-G-A

27983893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432815-T-A

27983893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432815-T-C

27983893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432815-T-G

27983904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432807-G-C

27983904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432807-G-T

27983925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432791-G-A

27983925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432791-G-C

27983925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432791-G-T

http://identifiers.org/hco/22/GRCh38#27983983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111432731-C-A

27984080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432690-C-G

27984381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432593-A-T

27984402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432579-T-G

27984456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432551-C-G

27984465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432542-C-T

27984664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432416-C-G

27984885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111432208-T-C

27985100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431994-T-A

27985100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431994-T-C

27985105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431989-A-T

http://identifiers.org/hco/22/GRCh38#27985141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431960-A-C

27985141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431960-A-G

http://identifiers.org/hco/22/GRCh38#27985192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431943-C-A

27985192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431943-C-G

27985192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431943-C-T

http://identifiers.org/hco/22/GRCh38#27985193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431942-C-A

27985193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431942-C-T

http://identifiers.org/hco/22/GRCh38#27985402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431788-C-A

27985405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431785-G-C

27985405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431785-G-T

http://identifiers.org/hco/22/GRCh38#27985420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431770-C-A

27985420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431770-C-T

27985421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431769-G-A

27985421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431769-G-C

27985421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431769-G-T

27985491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111431732-T-C

27985715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111431587-T-C

http://identifiers.org/hco/22/GRCh38#27985727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431575-A-C

27985797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111431513-G-A

http://identifiers.org/hco/22/GRCh38#27985901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431422-C-A

27985901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111431422-C-G

http://identifiers.org/hco/22/GRCh38#27985916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431407-C-A

27985954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111431375-T-C

http://identifiers.org/hco/22/GRCh38#27986026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111431303-A-C

27986026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111431303-A-G

27989865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111430778-A-T

27990015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111430630-A-G

27990134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111430540-T-C

27990187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111430332-T-C

27990187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111430332-T-G

27990334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111430145-C-T

27990365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111430100-A-G

http://identifiers.org/hco/22/GRCh38#27990714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111429845-C-A

27990714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111429845-C-G

27990740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111429814-G-A

27990740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111429814-G-T

27990915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111429633-A-G

27991283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111429433-G-C

27991422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111429306-A-G

27991727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111429028-C-G

http://identifiers.org/hco/22/GRCh38#27992460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428719-C-A

http://identifiers.org/hco/22/GRCh38#27992471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428714-C-A

27992499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428679-A-G

27992499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428679-A-T

27992516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428664-G-T

27992523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428659-T-G

27992536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428646-C-T

http://identifiers.org/hco/22/GRCh38#27992749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428488-A-C

27992830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428409-T-C

http://identifiers.org/hco/22/GRCh38#27992873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428381-C-A

27992873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428381-C-T

http://identifiers.org/hco/22/GRCh38#27992905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428367-C-A

27992905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428367-C-G

27992905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428367-C-T

http://identifiers.org/hco/22/GRCh38#27992936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428335-C-A

27992936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428335-C-T

http://identifiers.org/hco/22/GRCh38#27992937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428334-A-C

27992937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428334-A-T

http://identifiers.org/hco/22/GRCh38#27992950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428318-C-A

http://identifiers.org/hco/22/GRCh38#27992965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428306-C-A

27992965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428306-C-T

27992972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428299-A-G

27992972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428299-A-T

27993069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428224-A-G

27993070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428223-G-C

27993070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428223-G-T

http://identifiers.org/hco/22/GRCh38#27993152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428137-C-A

27993152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428137-C-T

http://identifiers.org/hco/22/GRCh38#27993224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428079-C-A

27993261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428069-G-A

27993261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428069-G-T

http://identifiers.org/hco/22/GRCh38#27993262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111428068-C-A

27993262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111428068-C-T

27993349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111427992-A-G

27993385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111427956-T-A

27993475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111427866-G-A

27993511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111427830-T-A

27993539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111427806-A-G

http://identifiers.org/hco/22/GRCh38#27993555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111427790-C-A

27993555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111427790-C-T

27993562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111427783-G-T

http://identifiers.org/hco/22/GRCh38#27996141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111426458-C-A

27996141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111426458-C-T

27998565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111425343-G-A

27998565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111425343-G-T

27998674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111425234-A-G

http://identifiers.org/hco/22/GRCh38#27998890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111425018-C-A

27998890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111425018-C-T

27998938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111424970-C-T

http://identifiers.org/hco/22/GRCh38#27999103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#111424805-C-A

27999106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111424802-A-G

http://identifiers.org/hco/22/GRCh38#28000074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111424499-C-A

28000074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424499-C-T

28000095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424479-G-A

28000095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424479-G-T

28000111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424461-G-A

28000130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424451-A-G

28000161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111424420-A-G

28001402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 111424177-G-A

28001411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 111424168-G-C

28001479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 111424100-G-A

http://identifiers.org/hco/22/GRCh38#28001650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111423958-C-A

28001650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111423958-C-T

28001680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423931-G-A

http://identifiers.org/hco/22/GRCh38#28001706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111423925-C-A

28001706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423925-C-T

28001749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423882-C-T

28001818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423840-A-T

28001839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423819-G-A

28001839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423819-G-T

28002008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423520-G-C

28002012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423516-T-C

28002051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423476-T-C

28002121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423412-A-G

28002135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423398-T-A

28002135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423398-T-C

28002142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423391-A-G

http://identifiers.org/hco/22/GRCh38#28002209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111423322-C-A

28002209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111423322-C-T

28002387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423107-G-A

28002387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423107-G-T

28002401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423088-T-A

28002401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423088-T-C

http://identifiers.org/hco/22/GRCh38#28002417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111423052-C-A

28002427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111423032-G-A

http://identifiers.org/hco/22/GRCh38#28002587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111422856-C-A

http://identifiers.org/hco/22/GRCh38#28002598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111422845-C-A

28002600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111422843-T-C

28002675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111422780-G-A

http://identifiers.org/hco/22/GRCh38#28002677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111422778-C-A

http://identifiers.org/hco/22/GRCh38#28002714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#111422744-C-A

28002714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111422744-C-T

28006537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29336
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111422439-G-T