http://identifiers.org/hco/7/GRCh38#32957619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56809237-C-A

32957619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56809237-C-T

http://identifiers.org/hco/7/GRCh38#32957666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56809284-C-A

32957666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56809284-C-T

32957692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56809310-G-A

32957692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56809310-G-C

32957692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56809310-G-T

http://identifiers.org/hco/7/GRCh38#32957789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56809407-C-A

32957789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56809407-C-G

32957789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56809407-C-T

http://identifiers.org/hco/7/GRCh38#32957801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56809419-C-A

32957801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56809419-C-T

32957908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809459-T-A

32957908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809459-T-C

32957943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809482-A-G

32957943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809482-A-T

32957998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809513-G-A

32958153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809637-G-C

32958161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809645-C-G

32958340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56809831-G-A

32958517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56810004-T-C

32960519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56811011-T-C

32960640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56811116-G-A

32960678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56811139-A-G

32961084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56811462-A-G

32961085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56811463-T-C

32962680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813235-G-A

32962680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813235-G-T

32962704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813259-T-C

32962768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813323-G-C

32962796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813344-A-G

32963004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56813539-A-G

32963533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56814600-T-C

http://identifiers.org/hco/7/GRCh38#32963536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56814603-C-A

32963536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56814603-C-T

32963538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56814605-T-C

32963538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56814605-T-G

32963716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814774-T-C

32963728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814786-G-A

32963728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814786-G-T

32963820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814832-G-A

32963820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814832-G-C

32963822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814834-G-A

32963822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814834-G-T

32963883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56814897-G-T

32964008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56815020-C-T

32964292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56815265-C-T

32964582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56815480-C-T

32964922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56815770-A-G

32966264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56817258-G-A

32970456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56819890-A-G

32970465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56819899-G-A

http://identifiers.org/hco/7/GRCh38#32970843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56820187-C-A

32970868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56820207-A-G

32970868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56820207-A-T

32971182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56820520-G-C

32971943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823378-A-G

32972142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823584-A-G

32972149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823590-G-A

32972216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56823642-G-A

32972297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823719-T-A

32972364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823771-G-A

32972478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823862-A-G

32974405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826429-T-C

32974443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826471-C-G

32974467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826495-G-T

32974470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826498-A-T

32974471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826499-T-C

http://identifiers.org/hco/7/GRCh38#32974547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56826557-A-C

32974551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826561-T-G

32974565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826571-G-A

32974566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826572-A-G

http://identifiers.org/hco/7/GRCh38#32974909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56826888-C-A

32974958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56826932-G-A

32974958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56826932-G-T

32975000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56826970-T-C

32975056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56827012-G-A

32975056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56827012-G-T

32975064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56827020-T-C

http://identifiers.org/hco/7/GRCh38#32975158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56827522-C-A

32975158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56827522-C-T

32975219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56827585-T-G

32975237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56827603-T-C

32975261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56827627-G-A

32975261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56827627-G-C

32975428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827783-T-C

http://identifiers.org/hco/7/GRCh38#32975430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56827785-C-A

32975439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827794-T-G

32976119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828142-G-C

32976141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828153-G-A

32976241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828242-A-T

32976299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828297-G-A

32976317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828307-T-C

32976372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56828365-A-G

32976381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56828374-G-A

32976381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56828374-G-T

32976483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 56828476-T-G

http://identifiers.org/hco/7/GRCh38#32976507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56828500-C-A

32976507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56828500-C-T

32976564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828797-A-G

http://identifiers.org/hco/7/GRCh38#32976580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56828812-A-C

32976580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828812-A-T

32976591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828823-C-G

32976744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828981-T-C

32976752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828989-C-T

32976772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829010-C-T

32977030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829254-G-A

32978782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831324-A-G

32979996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833030-C-T

32980215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833082-T-C

32980215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833082-T-G

32980374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833228-T-C

32980374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56833228-T-G

http://identifiers.org/hco/7/GRCh38#32980377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56833231-C-A

32980377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833231-C-G

32980377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833231-C-T

32980497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56833351-C-G

32980497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833351-C-T

32980533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833387-T-C

http://identifiers.org/hco/7/GRCh38#32980539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56833393-C-A

32980539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56833393-C-T

32980620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833468-A-T

32980634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833482-A-T

http://identifiers.org/hco/7/GRCh38#32980685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56833524-C-A

32980685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833524-C-T

32981021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833621-C-T

32981118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833700-G-A

32981320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833855-C-T

32981552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834059-G-T

32981597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834103-G-A

32981627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834137-G-C

32981700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834215-C-T

http://identifiers.org/hco/7/GRCh38#32981955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56834526-C-A

http://identifiers.org/hco/7/GRCh38#32981983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56834545-A-C

32981983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834545-A-G

32981983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834545-A-T

32982241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834760-G-A

http://identifiers.org/hco/7/GRCh38#32982269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56834786-A-C

32982272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834789-C-T

32982473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835011-C-T

32982652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835180-C-G

32988372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56837507-G-A

32988372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56837507-G-T

32988458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56837592-T-G

http://identifiers.org/hco/7/GRCh38#32988669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#56837797-C-A

32988669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56837797-C-T

32988672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56837800-G-A

32988702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56837828-A-G

32988702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56837828-A-T

32988735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56837951-T-C

32988934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56838159-G-A

32988934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56838159-G-T

32988960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56838184-T-C

32988977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56838193-T-A

http://identifiers.org/hco/7/GRCh38#32988998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56838225-C-A

32988998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56838225-C-T

32989061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838252-A-G

32989093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838276-A-G

32990736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839823-A-G

32990886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839982-C-T

32990931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840027-T-C

32990934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840030-C-T

32991113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841056-T-A

32991271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841257-G-A

32991539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841443-A-G

32991885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841751-A-G

32991990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56842056-T-C

32992727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 56842371-G-T

32992839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842481-A-G

32992841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842483-A-G

32992855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842497-T-C

32992862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842504-G-A

32992862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842504-G-T

http://identifiers.org/hco/7/GRCh38#32992909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56842551-C-A

32992909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842551-C-T

32992910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842552-T-C

32992910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842552-T-G

32993057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842700-A-G

32993057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56842700-A-T

32993075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56842717-G-T

http://identifiers.org/hco/7/GRCh38#32993163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56842797-A-C

32996056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845617-G-A

32996056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845617-G-T

http://identifiers.org/hco/7/GRCh38#32996066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56845627-C-A

32996066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845627-C-G

32996209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56845751-C-T

http://identifiers.org/hco/7/GRCh38#32996458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56845977-C-A

32996458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845977-C-T

http://identifiers.org/hco/7/GRCh38#32996462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56845981-C-A

32996462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845981-C-G

32996462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845981-C-T

32996477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845996-G-A

32996477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845996-G-C

32996499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846014-G-A

http://identifiers.org/hco/7/GRCh38#32996596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56846108-A-C

32998097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847009-T-G

http://identifiers.org/hco/7/GRCh38#32998227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56847102-A-C

32998227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847102-A-G

32998392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847215-T-C

http://identifiers.org/hco/7/GRCh38#32998583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#56847415-C-A

32998583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56847415-C-T

32998652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56847487-G-C

32998652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56847487-G-T

http://identifiers.org/hco/7/GRCh38#32998655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#56847490-C-A

32998944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849148-T-G

32999060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849262-G-A

32999214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849447-C-T

32999275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849506-C-G

32999275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849506-C-T

32999280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849511-G-A

http://identifiers.org/hco/7/GRCh38#32999281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56849512-C-A

32999339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849571-C-T

32999345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849577-G-A

32999502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849690-T-C

32999502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849690-T-G

32999504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849692-C-T

32999584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849729-A-G

32999584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849729-A-T

32999755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56849919-G-A

32999781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850048-C-G

32999805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850079-C-T

http://identifiers.org/hco/7/GRCh38#32999810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56850084-C-A

32999810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850084-C-T

http://identifiers.org/hco/7/GRCh38#32999816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56850092-C-A

32999818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850094-C-G

32999965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850256-T-G

32999989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850280-A-G

33000005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850287-T-A

33000348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850575-G-A

33000348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850575-G-T

33000410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850650-T-C

33002608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852592-G-A

33002608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852592-G-T

33002618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852597-T-C

http://identifiers.org/hco/7/GRCh38#33002623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56852602-C-A

33002640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852619-G-A

33002640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852619-G-C

33002650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852629-G-A

33002650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852629-G-T

33002923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56852870-G-A

33002923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56852870-G-T

33003055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852974-G-A

33003055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852974-G-T

33003127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853046-A-G

33003397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853311-T-C

33004218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853987-C-T

33004300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854021-G-A

33004311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854030-T-A

33004463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854162-T-C

33004701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854382-G-A

33004980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56854629-G-A

33005367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855211-G-A

33005367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855211-G-C

33005373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855217-G-A

http://identifiers.org/hco/7/GRCh38#33005400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855244-C-A

http://identifiers.org/hco/7/GRCh38#33005457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855302-C-A

33005515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855361-G-T

http://identifiers.org/hco/7/GRCh38#33005522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855368-A-C

http://identifiers.org/hco/7/GRCh38#33005570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855415-C-A

http://identifiers.org/hco/7/GRCh38#33005571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855416-C-A

33005571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855416-C-G

33005605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855439-G-A

33005605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56855439-G-T

33005646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855479-T-A

33005768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855588-A-G

33005772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855592-T-G

33005795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855613-G-A

33005795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855613-G-T

33005811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855627-T-G

http://identifiers.org/hco/7/GRCh38#33005839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855655-C-A

33005839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855655-C-T

33005866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855682-G-A

33005866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855682-G-T

http://identifiers.org/hco/7/GRCh38#33005883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855703-C-A

33005883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855703-C-T

http://identifiers.org/hco/7/GRCh38#33005884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855715-C-A

33005884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855715-C-T

http://identifiers.org/hco/7/GRCh38#33005885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56855716-C-A

33005885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855716-C-T

33005963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855796-G-A

33005963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855796-G-T

33006044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56855885-T-C

http://identifiers.org/hco/7/GRCh38#33006648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56856073-C-A

33006648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56856073-C-T

http://identifiers.org/hco/7/GRCh38#33006682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56856107-C-A

33006752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: 56856163-G-T

http://identifiers.org/hco/7/GRCh38#33006896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3725
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#56856306-C-A