http://identifiers.org/hco/3/GRCh38#150762021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58598265-A-C

150762072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598302-A-G

http://identifiers.org/hco/3/GRCh38#150762083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58598311-A-C

150762083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598311-A-G

150762093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598321-T-C

150762121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598344-G-A

150762121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598344-G-T

150762162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598375-G-A

150762162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598375-G-C

150762162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598375-G-T

150762163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598378-G-A

150762163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598378-G-C

150762278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58598548-T-G

http://identifiers.org/hco/3/GRCh38#150762298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58598650-C-A

http://identifiers.org/hco/3/GRCh38#150762342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58598726-C-A

150762342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58598726-C-T

150762429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58598813-T-G

150762457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58598841-G-A

http://identifiers.org/hco/3/GRCh38#150762656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599040-C-A

150762656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599040-C-T

150762676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599060-G-A

150762676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599060-G-T

http://identifiers.org/hco/3/GRCh38#150762730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599114-A-C

150762730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599114-A-G

http://identifiers.org/hco/3/GRCh38#150762762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599146-C-A

150762762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599146-C-T

http://identifiers.org/hco/3/GRCh38#150762845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599232-C-A

150762845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599232-C-T

http://identifiers.org/hco/3/GRCh38#150762864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599251-A-C

150762864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599251-A-G

150763122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599489-G-A

150763122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599489-G-T

150763124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599491-G-A

150763124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599491-G-T

150763168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599535-G-A

150763168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599535-G-T

http://identifiers.org/hco/3/GRCh38#150763302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58599657-C-A

150763302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599657-C-T

150763396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599725-G-A

150763396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599725-G-T

150763416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599745-G-A

150763416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599745-G-T

150763428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58599758-A-G

150763541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58599873-G-A

150763541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58599873-G-T

150763556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58599888-G-A

150763772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58600049-A-G

150763773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58600050-G-T

150763892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58600164-G-C

150765084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602185-C-T

150765628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602669-C-G

150765656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602686-G-A

150765656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602686-G-T

150765891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602953-C-T

150765915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602975-G-A

150765915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58602975-G-T

150766238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58603291-C-T

150770298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58608492-G-C

150770496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58608703-G-A

150770925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58609454-A-T

150771071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58610173-T-C

150771137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58610282-C-T

150771138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58610283-G-A

150771217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58610361-C-T

http://identifiers.org/hco/3/GRCh38#150771285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58610435-C-A

150771441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58611226-G-A

150771441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58611226-G-C

150771498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58611290-G-A

150771498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58611290-G-C

150771704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611496-G-A

150771733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611524-G-A

150771826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611610-G-A

150771979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611664-A-G

150772379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611810-G-A

150772495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58611931-T-A

150772610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58612370-A-G

150773385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58612601-A-G

150775604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58613937-C-T

150775605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58613938-G-A

150775665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58613993-T-C

150775899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614277-A-G

150775903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614281-C-T

http://identifiers.org/hco/3/GRCh38#150775954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58614332-C-A

150775954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614332-C-T

150775971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614347-A-T

150776062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614443-T-C

150776072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614453-A-G

150776104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614485-T-G

150776310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614669-T-C

150776450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614790-A-G

http://identifiers.org/hco/3/GRCh38#150776461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58614800-C-A

150776467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614806-A-G

150776643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58614997-C-T

150776739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58615070-G-A

150776749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58615080-G-A

150777347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58615682-T-G

150777646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58615876-C-T

150777844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58616069-T-C

150780565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58627759-A-G

150780687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58627878-G-T

150780701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58627892-T-A

150780726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58627917-C-T

150780965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58628136-C-T

150781136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58628289-C-G

150781136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58628289-C-T

150783516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58630468-G-A

http://identifiers.org/hco/3/GRCh38#150783519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58630471-A-C

150783872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58630791-G-A

150783965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58630882-T-C

150784182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58631039-T-A

150784282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58631136-C-T

150784308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58631162-C-T

150784601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58631475-T-C

http://identifiers.org/hco/3/GRCh38#150786892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58633746-A-C

150786920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58633774-G-A

150787106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58633923-G-A

150787156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58633967-A-G

150787584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58634356-T-A

150787737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58634503-T-C

150787949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58634701-C-T

150788304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58634991-C-G

150788306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58634993-G-A

150788432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58635127-A-G

150788690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58635385-T-C

150789478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58636377-G-A

150789981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58636794-C-T

150790081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58636888-A-G

150790509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58637300-C-G

150790554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58637357-C-T

150791211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58638039-G-C

150791247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58638075-C-G

http://identifiers.org/hco/3/GRCh38#150791260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58638088-C-A

150791526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58638337-G-A

150794015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58638952-C-G

150794158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58639087-G-A

150794237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58639149-A-G

150794544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58639418-T-C

150798181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645828-C-T

150798230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645872-T-C

150798391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646004-G-A

150798391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646004-G-T

150798609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646203-G-A

150798736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646281-C-T

150798763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646309-G-A

150800024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650959-T-C

http://identifiers.org/hco/3/GRCh38#150803596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58655586-A-C

150803600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655590-C-T

150803699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655679-A-G

150803729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655705-A-G

150803802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655774-A-G

150803824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655795-A-G

150803841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655812-G-A

150804359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657330-A-G

http://identifiers.org/hco/3/GRCh38#150804536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58657526-C-A

150804536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657526-C-T

150804866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657865-G-A

150804868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657867-T-C

150804886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657885-T-C

150804905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657904-C-T

150805078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58658017-T-C

150805487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58658407-G-C

150805491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58658411-C-T

http://identifiers.org/hco/3/GRCh38#150805527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58658444-C-A

150805527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58658444-C-T

150806296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659554-C-T

150806297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659555-G-A

150806444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659705-C-G

150806705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660090-T-C

150806813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58660186-T-G

150806841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58660214-G-A

150806926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58660288-G-A

150807164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660516-T-C

150807187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660539-C-T

150807935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660595-G-A

150808961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661138-G-A

150809396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661711-G-A

150809396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661711-G-C

http://identifiers.org/hco/3/GRCh38#150809552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58661997-C-A

150809916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662307-T-G

150809934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662325-A-T

150812084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58668945-A-G

http://identifiers.org/hco/3/GRCh38#150828913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58681463-C-A

150830195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58683934-G-A

150830195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58683934-G-C

150830211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58683950-T-C

150830279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58684019-T-G

150830357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58684078-A-T

http://identifiers.org/hco/3/GRCh38#150830483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58684206-C-A

150830483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58684206-C-T

150830607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58684776-G-A

150865456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58692054-T-A

http://identifiers.org/hco/3/GRCh38#150865800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58692583-A-C

150865800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58692583-A-G

150866648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58693142-G-A

http://identifiers.org/hco/3/GRCh38#150866676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58693170-C-A

http://identifiers.org/hco/3/GRCh38#150869254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58695766-A-C

150869341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58695858-G-C

150869560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696098-A-G

150869673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696226-C-T

150869907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696437-A-G

http://identifiers.org/hco/3/GRCh38#150869954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58696497-A-C

150870136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696681-G-A

150870157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696706-C-T

150870194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58696740-T-G

150870541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697104-C-G

http://identifiers.org/hco/3/GRCh38#150870918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58697437-A-C

http://identifiers.org/hco/3/GRCh38#150870964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58697473-A-C

150870964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697473-A-G

150871005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697507-T-G

150871007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697509-C-T

150871117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58697613-T-C

150871547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58697930-T-A

150872478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698517-G-A

150872802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698746-T-C

150872816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698760-C-T

150873009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58698964-C-G

http://identifiers.org/hco/3/GRCh38#150873112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#58699053-C-A

150873167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699104-C-T

http://identifiers.org/hco/3/GRCh38#150873252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#58699189-C-A

150873252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58699189-C-T

150873478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699411-G-T

150873490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699423-G-A

150873490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58699423-G-T