http://identifiers.org/hco/21/GRCh38#32772112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90841542-A-C

32772112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841542-A-G

32772125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841555-G-A

32772125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841555-G-C

32772125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841555-G-T

32772127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841557-T-G

http://identifiers.org/hco/21/GRCh38#32772168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90841597-C-A

32772168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841597-C-G

32772168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841597-C-T

http://identifiers.org/hco/21/GRCh38#32772233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90841684-C-A

32772233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841684-C-G

32772233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841684-C-T

http://identifiers.org/hco/21/GRCh38#32772248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90841700-C-A

32772248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: non coding transcript exon variant
orthologous variants: 90841700-C-T

32772286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90841736-T-A

32772286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90841736-T-C

32772286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90841736-T-G

32772507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842003-T-C

32773622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843702-A-G

32773713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843793-A-G

32774273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843871-G-A

32774334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843925-G-C

32774348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843939-A-G

32777967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844352-A-G

32778272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844639-A-G

32778321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844682-T-C

32778400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844759-A-G

32778419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844778-G-A

32778480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844839-G-C

32778636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844993-A-G

32778677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845029-C-T

http://identifiers.org/hco/21/GRCh38#32778696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90845048-C-A

32778712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845064-G-A

32778715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845065-A-G

32778762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845105-G-A

32779913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90846644-T-C

32780488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90846773-A-T

32780596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847368-G-C

32780768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847519-A-T

32780771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847522-G-T

32781109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848003-G-A

32781159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848085-T-A

32781234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848168-T-C

32782634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848457-A-G

32782891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848717-A-G

32783029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848840-T-G

32791316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90850053-G-T

http://identifiers.org/hco/21/GRCh38#32791382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90850122-C-A

http://identifiers.org/hco/21/GRCh38#32791450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90850182-A-C

http://identifiers.org/hco/21/GRCh38#32791495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90850230-C-A

32791495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90850230-C-T

32791642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90850366-C-T

32791735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90850435-A-G

http://identifiers.org/hco/21/GRCh38#32792292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90850911-C-A

http://identifiers.org/hco/21/GRCh38#32792329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90850947-A-C

32792549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851133-G-A

32792606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851190-G-A

32792729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851339-C-G

32793242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851900-C-T

32793247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851905-G-A

32793483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852215-G-T

32793490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852222-A-G

32793535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852265-G-T

32793675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852351-A-G

http://identifiers.org/hco/21/GRCh38#32793685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90852361-C-A

32793685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852361-C-T

32793718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852402-T-G

32793736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852420-C-G

32793796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852476-C-G

32793796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852476-C-T

32793807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852487-G-A

32793915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852595-G-A

32793976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852638-T-C

32794070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852732-C-T

32794226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852888-C-T

32794262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90852924-A-G

32794381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 90853040-G-A

32794381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 90853040-G-C

32794515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853173-C-T

32794517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853176-T-C

32794540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853199-T-A

32794540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853199-T-C

http://identifiers.org/hco/21/GRCh38#32794580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90853233-C-A

32794580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853233-C-G

http://identifiers.org/hco/21/GRCh38#32794633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90853252-C-A

32794709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853325-G-A

32794801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853401-C-T

32795013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853624-A-G

32795015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853626-G-T

32795080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853687-A-G

32795235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853830-G-A

32795282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853877-A-G

32795331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853922-G-A

32795355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853931-T-C

32795362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90853938-C-T

32795529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854087-C-T

32795653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854203-G-A

32796417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854384-A-G

32796530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854492-T-C

32796715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854665-G-A

32796735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854685-C-T

32796810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854757-T-C

http://identifiers.org/hco/21/GRCh38#32796847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90854794-C-A

32796847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854794-C-G

32796847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854794-C-T

http://identifiers.org/hco/21/GRCh38#32796855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90854802-C-A

32796855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854802-C-G

32796887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854843-T-G

32796888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854844-C-G

32796888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854844-C-T

http://identifiers.org/hco/21/GRCh38#32796917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90854877-A-C

32796917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90854877-A-G

32796969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90854924-G-A

32797072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855014-G-A

http://identifiers.org/hco/21/GRCh38#32797095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90855032-C-A

32797095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855032-C-T

http://identifiers.org/hco/21/GRCh38#32797104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90855041-C-A

http://identifiers.org/hco/21/GRCh38#32797116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90855053-C-A

32797116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855053-C-T

http://identifiers.org/hco/21/GRCh38#32797159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90855091-C-A

32797188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855120-C-T

32797193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855123-T-C

32797236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855147-T-C

http://identifiers.org/hco/21/GRCh38#32797246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90855157-C-A

32797246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855157-C-T

32797257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855168-G-C

32797257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855168-G-T

32800335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858058-A-G

32800963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858306-C-T

32801060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90858398-G-A

32801177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90858514-C-T

http://identifiers.org/hco/21/GRCh38#32801446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90858760-C-A

32801574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90858833-C-G

32801937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90858913-G-T

32802107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859052-A-T

32802155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859100-G-T

32802205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859151-T-C

32802281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859210-A-G

32802353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859271-G-A

32802500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859396-A-G

32802651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859513-A-G

32802714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859574-A-T

32802752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859613-G-T

32803198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859916-C-G

32803524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861278-A-T

32803604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861351-T-C

32803612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861360-A-G

32803612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861360-A-T

32803751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861473-G-A

32803852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861562-T-C

32803882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90861581-G-A

32803882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90861581-G-T

32804021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861711-T-A

http://identifiers.org/hco/21/GRCh38#32804031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90861721-C-A

http://identifiers.org/hco/21/GRCh38#32804053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90861745-C-A

32804101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861789-G-A

32804223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861905-C-G

32812321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864956-C-T

http://identifiers.org/hco/21/GRCh38#32812552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90865176-C-A

32812552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865176-C-T

32812762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865341-T-C

http://identifiers.org/hco/21/GRCh38#32813024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90865417-C-A

32813214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865596-C-G

32813314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865666-G-A

32813354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865707-A-G

32813389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865741-G-A

http://identifiers.org/hco/21/GRCh38#32813479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90865826-C-A

http://identifiers.org/hco/21/GRCh38#32813607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#90865935-C-A

32813607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90865935-C-T

32813706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90866041-G-A

32813713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90866048-T-C

http://identifiers.org/hco/21/GRCh38#32813795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90866126-C-A

http://identifiers.org/hco/21/GRCh38#32813814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90866142-C-A

32813814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90866142-C-T

32813856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90866166-G-T

32813982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90866294-C-T

32813994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90866309-G-A

32814095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90866414-T-C

32815740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90867916-G-C

http://identifiers.org/hco/21/GRCh38#32826238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90869867-C-A

32826238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90869867-C-G

32826238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90869867-C-T

32826247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90869876-C-T

32826257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90869885-A-G

32826555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870161-G-A

32826622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870208-C-G

http://identifiers.org/hco/21/GRCh38#32826699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90870297-C-A

32826857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870674-G-A

32827113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870953-C-G

32827122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870962-G-T

32827128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90870968-G-A

32827760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90873306-G-C

32827955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90873486-T-C

http://identifiers.org/hco/21/GRCh38#32827972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90873503-A-C

32828251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90873828-C-G

32833307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90888635-T-C

32833328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90888656-C-T

32833930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90889754-G-A

32833930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90889754-G-T

32833968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90889792-C-T

32834030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90889860-A-G

32834296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90890146-A-G

http://identifiers.org/hco/21/GRCh38#32834429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90890273-A-C

32834522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90890436-C-T

32834676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90890841-A-T

32836938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891277-G-A

32836998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891337-A-G

32837126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891462-C-T

32837250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891601-T-C

32837283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891633-G-A

32837528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90891848-C-G

32837806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90892116-T-C

32838572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90892628-G-A

32838649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90892702-A-T

32838804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90892869-A-G

32839340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90893203-T-G

32839367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90893225-A-G

32839371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90893229-C-T

32840381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90894198-C-T

32840591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90894387-T-A

32840632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90894428-G-A

32840632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90894428-G-C

32840702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90894506-G-A

http://identifiers.org/hco/21/GRCh38#32843641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90895653-C-A

32843641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90895653-C-T

32844458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90896090-T-A

32844458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90896090-T-C

http://identifiers.org/hco/21/GRCh38#32844521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90896123-A-C

32844521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90896123-A-G

32844952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90896547-C-T

32845260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90896871-G-A

32845264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90896875-G-C

32845461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897077-G-T

32845487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897103-T-A

32845487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897103-T-C

32845998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897768-A-G

32846112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897865-G-A

32846176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90897929-C-T

32846334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90898084-G-C

32847148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90899055-A-G

32847380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90899594-C-T

32847940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900168-G-A

32848006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900235-C-T

32848022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900244-G-A

32848061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900346-G-A

32848321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900503-C-T

32848334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900508-C-T

32848376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900555-C-T

32848389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900568-A-G

32848399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900578-G-T

32848463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900627-A-G

32848717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90900960-T-G

32848776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90901020-T-C

http://identifiers.org/hco/21/GRCh38#32848958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90901155-C-A

32848973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90901170-G-A

http://identifiers.org/hco/21/GRCh38#32849298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90901492-C-A

32849806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90901991-G-A

32849806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90901991-G-T

32850728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90902964-T-A

32851073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90903307-A-T

32851075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90903309-A-G

32851144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90903387-T-A

32851185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90903428-T-C

32851380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90903566-A-G

32851760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904432-G-A

http://identifiers.org/hco/21/GRCh38#32851928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90904572-C-A

32852021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904616-G-A

32852021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904616-G-C

32852021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904616-G-T

32852024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904618-G-A

http://identifiers.org/hco/21/GRCh38#32852141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90904727-C-A

32852141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904727-C-T

32852144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904730-A-G

32852239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904824-G-A

32852239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904824-G-T

32852311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904881-T-C

32852325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904895-G-A

32852325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904895-G-T

http://identifiers.org/hco/21/GRCh38#32852371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90904947-C-A

32852371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90904947-C-T

32861332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90907832-T-G

32861908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90908110-C-T

32861951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90908142-C-T

32862638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90909474-T-C

32862818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90909747-C-G

32863178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90910045-G-A

32863178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90910045-G-C

http://identifiers.org/hco/21/GRCh38#32863261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90910128-A-C

32863422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90911710-T-A

32864786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90912442-T-C

32864811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90912469-C-T

32865143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90912972-C-T

http://identifiers.org/hco/21/GRCh38#32865187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90913012-C-A

32865285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90913135-G-A

32865540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90913401-G-T

http://identifiers.org/hco/21/GRCh38#32867975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90916506-C-A

http://identifiers.org/hco/21/GRCh38#32868388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90916910-C-A

32868496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90917014-T-C

32868920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90918160-C-T

32868921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90918161-A-G

32868962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90918200-C-G

32868962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90918200-C-T

32879842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922111-G-A

32879842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922111-G-C

32879862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922132-C-T

32879994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922222-A-G

32879999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922227-C-T

http://identifiers.org/hco/21/GRCh38#32880062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90922290-A-C

32880360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922601-T-A

32880447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922684-G-A

32880463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90922700-C-T

32880528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90922744-C-T

32880641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90922841-G-A

32880641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90922841-G-C

http://identifiers.org/hco/21/GRCh38#32880668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90922868-C-A

32880668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90922868-C-G

32880674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90922874-T-C

32880867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90923026-G-A

32880940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90923092-C-T

32881712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90924390-T-A

32881974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90924614-C-T

32889356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90925080-C-T

32889463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90924970-G-C

32889476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90924952-G-A

32910559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90932715-A-G

32910578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90932735-A-G

32913985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90933177-C-G

32914279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90933440-G-T

32914398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90933540-G-A

32914508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90933650-C-T

32914991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934155-A-G

32914992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934156-A-G

32914992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934156-A-T

32915044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934203-T-A

32915238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934365-A-G

32915282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934406-G-A

32915282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934406-G-T

http://identifiers.org/hco/21/GRCh38#32915492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90934988-C-A

32915492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90934988-C-T

32915534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935025-G-A

32915534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935025-G-C

32915659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935123-T-A

32915659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935123-T-C

32915760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935210-C-T

32915771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935225-G-A

32915771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935225-G-C

32915794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935247-T-C

32915927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90935417-G-A

32916641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90936027-T-C

32917573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90936519-C-G

32917635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90936566-A-G

32918677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90937225-G-T

32918755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90937314-C-T

32919201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90937767-T-A

32919264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90937805-T-A

32919282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90937823-A-G

32919506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938050-G-A

32919510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938054-C-T

32919548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938092-T-C

32919555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938099-A-G

32919798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938292-T-A

32920336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938717-G-C

32920357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938738-A-G

32920411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90938787-A-G

32923846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90941507-A-G

32923944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90941615-C-T

32924086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90941749-T-C

32924186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90941874-G-A

32924204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90941911-G-A

32924648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90942737-T-C

32925212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943493-T-C

32925233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943513-G-A

32927840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943686-T-C

32927985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943830-T-A

32928038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943870-C-T

32928080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943910-T-A

32928108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90943939-T-G

32928476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90944021-T-C

32928478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90944023-C-G

32928702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90944192-G-A

32928804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90944329-G-A

http://identifiers.org/hco/21/GRCh38#32929972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90945031-A-C

32931027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950020-G-C

32931027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950020-G-T

32931048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950041-T-C

32931146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950138-A-G

32931305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950248-G-A

http://identifiers.org/hco/21/GRCh38#32931519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90950383-C-A

32931596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950460-G-A

http://identifiers.org/hco/21/GRCh38#32931646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90950502-C-A

32931647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90950503-T-C

32932710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90953325-T-C

32933665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90953970-C-T

http://identifiers.org/hco/21/GRCh38#32933734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90954024-A-C

http://identifiers.org/hco/21/GRCh38#32933806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90954105-C-A

32933979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90954246-G-C

32933979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90954246-G-T

32940700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90957827-G-A

32940817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90957918-C-T

32940989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90958073-C-G

32940989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90958073-C-T

32941192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90958294-T-A

32941192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90958294-T-G

32942128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90959653-G-A

32942865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90959809-A-G

32942956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90959905-C-T

32943644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960217-T-C

32943836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960382-G-T

32943845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960390-G-A

32943862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960408-C-G

32943980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960496-C-T

32944066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960604-A-G

32944074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960629-T-C

32944692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90960915-G-T

32944856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961087-C-T

32944917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961149-G-A

32945028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961256-T-C

32945224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961413-G-A

32945296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961453-G-T

32945459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961583-C-T

32945609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90961737-C-T

http://identifiers.org/hco/21/GRCh38#32946062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90962784-C-A

32950599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90964874-C-T

32950620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90964893-C-T

32950669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90964910-C-T

32950884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965163-C-T

32950895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965174-T-G

32950897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965176-T-C

32950944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965245-C-T

http://identifiers.org/hco/21/GRCh38#32951123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90965425-C-A

32951217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965511-C-T

http://identifiers.org/hco/21/GRCh38#32951244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90965537-C-A

32951344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965662-T-G

32951381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965702-G-A

32951394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90965715-C-T

32952929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90967296-G-A

32953029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90967565-G-C

32953783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968029-A-G

32953799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968044-A-G

32953902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968168-G-A

http://identifiers.org/hco/21/GRCh38#32953903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90968169-A-C

32953915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968181-G-T

32954009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968848-C-T

32954011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968850-A-G

32954126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90968971-G-A

32954393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969241-C-T

32954394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969242-G-A

32954404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969256-G-A

32954441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969289-A-G

32954751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969574-G-C

32954790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90969613-T-C

32955584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90970452-C-T

32955756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90970643-G-A

32955756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90970643-G-C

32955756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90970643-G-T

32955919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90970823-G-A

32955955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90970857-G-A

32956209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90971152-G-A

http://identifiers.org/hco/21/GRCh38#32956237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90971158-C-A

32956396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90971292-A-G

32956550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90971400-A-G

32957434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972652-G-A

32957601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972814-G-A

32957601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972814-G-C

32957606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972819-T-A

32957638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972846-G-A

http://identifiers.org/hco/21/GRCh38#32957704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90972910-A-C

32957764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90972970-G-A

32957934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90973135-T-A

32958104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90973296-G-A

32962594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90975879-G-C

32962943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90976556-A-T

32962974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90976587-T-C

32965133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90977815-A-G

32965655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90978282-A-G

32965717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90978339-T-C

32965913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90978531-A-T

32970137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90980770-T-C

32970186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90980821-T-A

32970193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90980828-A-G

32970472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90980975-G-A

32971188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90981267-T-G

32971282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90981359-A-G

32971561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90981628-C-T

32972106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90983742-A-G

http://identifiers.org/hco/21/GRCh38#32972122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90983757-A-C

32972143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90983779-C-G

32972674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984272-A-G

32972793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984343-T-C

32972867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984416-C-T

32973125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984679-A-T

32973208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984744-A-G

32973241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90984773-A-G

32975873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987138-T-C

32976149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987379-T-C

32976153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987383-G-A

32976341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987559-G-A

32976446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987612-G-A

32976564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987904-A-G

32976571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90987911-T-C

http://identifiers.org/hco/21/GRCh38#32976988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90988418-C-A

http://identifiers.org/hco/21/GRCh38#32977364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#90988810-A-C

32977863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90989136-C-T

32977876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90989149-G-A

32978093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90989361-C-T

32978851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990121-T-C

32978870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990140-G-A

32979113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990395-G-A

32979422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990710-G-A

32979422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990710-G-C

32979429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990717-C-T

32979430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990718-G-A

32979430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990718-G-C

32979658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990903-A-G

32979681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90990924-G-T

32979825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991090-G-T

32979890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991141-G-A

32979904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991155-A-G

32979906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991157-G-A

32979910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991161-G-A

32980181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991341-C-T

32980345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991518-C-T

32980557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90991701-A-G

http://identifiers.org/hco/21/GRCh38#32991303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#91003106-C-A

32991563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91003360-C-G

32991586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91003383-C-T

32991677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91003473-C-G

33007815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91005331-T-A

33007815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91005331-T-C

33007918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91005411-T-C

33008026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91005511-T-C

33008649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006260-G-C

33009032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006651-G-A

33009101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006714-A-G

33009208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006820-G-C

33009240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006854-G-A

33009290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006931-G-C

33009290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006931-G-T

33009349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91006991-A-G

33009461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91007097-A-G

33009989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008248-C-T

33010070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008336-A-T

33010089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008354-A-G

33010197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008437-C-T

33010427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008668-G-A

33010464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008705-G-A

33010485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008731-C-T

http://identifiers.org/hco/21/GRCh38#33010612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#91008877-C-A

33010683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91008928-T-G

33010824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91009052-T-C

33014122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91011351-A-G

33014140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91011369-C-T

33014182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91011404-G-A

33015540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91011781-G-T

33016116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014275-C-T

33016134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014293-G-A

33016293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014456-C-T

http://identifiers.org/hco/21/GRCh38#33016406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#91014591-C-A

33016406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014591-C-T

33016491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014657-C-G

33016624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014784-C-T

33016719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1290
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91014840-G-C