46396419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91749186-G-A

46396419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91749186-G-T

http://identifiers.org/hco/11/GRCh38#46396672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91748935-C-A

46396754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748851-T-C

http://identifiers.org/hco/11/GRCh38#46396855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91748752-C-A

46396855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748752-C-T

46396955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748665-G-C

46396955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748665-G-T

46397001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748609-G-T

46397131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91748480-G-A

46397700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91747913-G-A

46397701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91747912-G-T

http://identifiers.org/hco/11/GRCh38#46398016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91747599-C-A

46398016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91747599-C-T

46398060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91747522-G-C

46399758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91747085-T-C

46399796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91747047-G-A

46399881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91746994-G-A

46399966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91746926-C-T

46402012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91745556-G-A

http://identifiers.org/hco/11/GRCh38#46402240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91745382-C-A

46402240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91745382-C-T

46402765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91745199-G-A

46403090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91744897-T-C

46403105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91744882-A-T

46403161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91744839-A-G

46403646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91744367-G-A

46404353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743900-G-C

46404373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743880-G-A

46404739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743559-C-T

46404816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743482-C-G

46404816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743482-C-T

46405041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91743280-C-T

46405382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91742999-C-G

46408459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741975-T-C

46408575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91741888-G-A

46408771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741699-C-T

46408823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741662-A-G

46408823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741662-A-T

46409555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741615-C-G

46409958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91741186-G-A

46410223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740803-G-A

46410232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740794-A-T

46410236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740781-G-A

46410265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740748-C-T

46410414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740592-G-A

46410453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740556-T-A

46410453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91740556-T-C

46412955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91736712-A-G

http://identifiers.org/hco/11/GRCh38#46413092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91736578-A-C

46413092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91736578-A-G

46413412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91736310-T-C

46415444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91734658-G-A

46418027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91730866-A-G

46418133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91730769-A-G

46419931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91728648-G-A

http://identifiers.org/hco/11/GRCh38#46422258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91727839-C-A

46422319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91727779-A-G

46422351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91727749-G-A

46422365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91727735-T-A

http://identifiers.org/hco/11/GRCh38#46423086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91727003-C-A

46429794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91721733-G-C

46429932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91721596-G-C

46429980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91721553-T-C

46430448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720409-A-G

46430518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720356-C-T

46430580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720300-T-G

http://identifiers.org/hco/11/GRCh38#46430667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91720214-C-A

46430711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720171-A-G

46430830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720054-T-C

46430888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91720000-T-C

46431205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91719535-T-C

46432601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91718314-G-A

46432848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717999-C-T

46432877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717970-C-T

46433165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717621-T-C

46433197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717590-G-A

46433436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717343-A-T

46433773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91717025-T-C

46434643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91716373-G-A

http://identifiers.org/hco/11/GRCh38#46434711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91716283-C-A

46434711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91716283-C-T

46434725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91716269-T-C

46434746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91716240-A-G

46435064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715921-G-T

46435083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715902-G-T

46435102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715882-G-C

46435118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715866-G-T

46435463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715555-C-T

46435617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715459-C-T

46435806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715250-T-C

46435850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91715208-A-T

46436250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91714800-T-C

46436494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91714571-T-A

46436705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91714404-C-T

46436926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91713696-G-A

46437352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91713051-A-G

46437568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91712858-T-G

46438703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91711665-G-A

46438703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91711665-G-T

46438714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91711656-T-C

46438761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91711605-A-G

46438951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91710920-A-G

46438957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91710903-A-G

46439306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91710459-A-T

46439793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91709985-G-C

46439961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91709847-A-G

46443718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705926-G-A

46443718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705926-G-T

46443724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705920-A-G

http://identifiers.org/hco/11/GRCh38#46443862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91705806-C-A

46443862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705806-C-T

46443863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705805-G-A

46443863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91705805-G-T

46445244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91704111-G-A

46445244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91704111-G-T

46445730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91701763-G-A

46445935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91701574-A-G

46446040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91701489-T-C

46446143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91701405-T-C

46446460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91701087-C-T

46451386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91695350-T-C

http://identifiers.org/hco/11/GRCh38#46451678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91695064-C-A

46451679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91695063-T-C

46451858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91694819-A-G

http://identifiers.org/hco/11/GRCh38#46451879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#91694798-A-C

46451879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91694798-A-G

46451943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91694652-G-A

46451943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91694652-G-T

46451989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91694598-G-T

46456216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91690578-T-C

46457123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91689687-A-G

46457299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91689529-G-T

46459895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91687433-C-T

46461355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91685568-A-G

46461576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91685391-G-T

46462380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91684760-A-G

46462917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91684269-C-T

46462945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91684246-G-C

46462961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91684230-C-T

46463035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91684137-T-C

46465278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91682199-G-T

46465562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91681969-G-A

46465794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91681738-A-G

46466278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91681252-C-T

46475635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91677525-G-A

46475717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91677453-T-C

46476101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91676529-C-T

46476509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91676004-T-C

http://identifiers.org/hco/11/GRCh38#46477722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91675194-A-C

46480813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91671945-A-G

46480876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91671883-A-G

46481145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91671629-G-A

46481660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91670973-G-A

46482374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91670291-G-A

46483327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91667699-A-G

46483513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91667521-A-G

46484371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91666430-T-C

46484507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91665910-A-G

46485955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91662855-T-C

46486062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91662757-T-C

46487866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91661477-T-C

46487899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91661422-T-C

46488650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91660542-T-C

46488781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91660424-A-G

46489515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91660075-C-T

46490294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91659356-G-C

46490827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91658863-T-C

46490883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91658807-T-C

46491124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91658561-T-C

46491241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91658462-T-C

46491339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91658354-T-C

46491349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91658341-G-T

46491855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91657828-G-A

46492260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91657294-T-G

46492330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91657154-T-C

46492435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91656896-A-G

46493494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655802-A-G

46493501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655797-A-G

46493507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655791-A-T

46493509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655789-G-A

46493509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655789-G-T

46493521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655777-T-C

46493533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655765-A-T

http://identifiers.org/hco/11/GRCh38#46493791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91655401-C-A

46493791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91655401-C-T

http://identifiers.org/hco/11/GRCh38#46493976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91655114-C-A

46493976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655114-C-G

46493976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655114-C-T

46493977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655113-G-A

46493977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655113-G-T

46494019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91655073-G-T

46494102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91654904-T-C

http://identifiers.org/hco/11/GRCh38#46494223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91654784-C-A

http://identifiers.org/hco/11/GRCh38#46494276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91654730-C-A

46494794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91654190-C-T

46494804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91654180-T-C

46494823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91654161-A-G

46494894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91654120-C-G

46495145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653898-C-T

46495253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653791-G-A

46495253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653791-G-C

46495253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653791-G-T

46495338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653713-A-G

46495348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653702-T-C

46495352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653698-T-C

46495455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91653621-A-G

46496744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91652336-T-A

46497124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91652009-T-A

46497288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91651841-T-C

46497635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91651483-C-T

http://identifiers.org/hco/11/GRCh38#46497812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91651344-A-C

46497875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91651295-G-C

46497912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91651262-T-C

46498282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91650942-G-A

46498286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91650938-T-C

46498466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91650755-G-A

46498752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91650480-T-C

46500192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91649283-A-G

46500345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91649146-C-T

46500624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91648478-T-C

46504471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91644344-G-T

46504697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91644123-A-G

46504794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91644033-T-A

46504957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91643422-T-G

46505313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91642564-A-G

46505543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91642336-G-A

http://identifiers.org/hco/11/GRCh38#46505666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91642228-C-A

46505666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91642228-C-T

http://identifiers.org/hco/11/GRCh38#46506089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91641650-C-A

46506089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91641650-C-T

46508125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91640615-T-C

46508177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91640566-G-A

46508177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91640566-G-T

46508388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91640355-G-A

46508818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91639943-A-G

46508854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91639905-C-T

46509305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91639312-G-C

46509305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91639312-G-T

46509720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91638726-T-C

46510251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91638061-A-G

46510367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91637960-T-G

46510813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91637493-T-C

46512153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91635967-G-A

46512153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91635967-G-C

46512411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91635751-T-A

46512606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91635574-T-C

46513305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91634915-A-T

46513645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91634685-T-C

46516080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91632479-T-C

46516241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91632306-A-G

46516350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91632201-C-T

46516849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91632031-G-A

46516896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631970-C-T

46517500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631652-G-A

46517500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631652-G-T

46517501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631651-T-A

46517501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631651-T-G

46517998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631473-G-T

46518041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91631420-T-C

46518188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 91631221-G-A

46518188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91631221-G-T

46518316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91631109-G-A

46518316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91631109-G-T

46518347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91631079-A-G

46518347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91631079-A-T

http://identifiers.org/hco/11/GRCh38#46518594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91627554-C-A

46521153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91625217-G-A

46521211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91625159-C-T

46522113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91624255-G-A

46522113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91624255-G-C

46522114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91624254-T-C

46522453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91624029-T-A

46523164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91622974-T-G

46523487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91622640-A-G

46524926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91621465-C-T

46528744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91619464-G-A

http://identifiers.org/hco/11/GRCh38#46528797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91619438-A-C

46529111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91619151-T-C

46529340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91618949-T-C

46529499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91618794-G-T

46529581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91618725-T-A

46529581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91618725-T-C

46529988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91617795-C-T

46530371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91617414-G-A

46530371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91617414-G-C

46535006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91614354-T-C

46535241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91614155-T-A

46535380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91614027-A-G

46535797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91613133-G-A

46535868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91613065-T-A

46536531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91611147-A-G

46536602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91611070-G-A

46538449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91608311-A-T

46539013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91607610-T-C

46540471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91606012-G-T

http://identifiers.org/hco/11/GRCh38#46540974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91605136-A-C

46540974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91605136-A-G

http://identifiers.org/hco/11/GRCh38#46541716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#91604314-C-A

http://identifiers.org/hco/11/GRCh38#46542731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91603304-C-A

46542731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91603304-C-T

46543200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91602832-G-A

46543200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91602832-G-T

46543203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91602829-G-A

46543203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91602829-G-T

http://identifiers.org/hco/11/GRCh38#46543452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91602588-C-A

46543452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91602588-C-T

http://identifiers.org/hco/11/GRCh38#46543538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91602498-A-C

46543953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91601339-T-A

46543953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91601339-T-C

46543963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91601330-G-A

46544082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91601226-G-A

46544082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91601226-G-T

46545834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91599199-G-A

46545834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91599199-G-C

46545834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91599199-G-T

46545871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91598703-T-A

http://identifiers.org/hco/11/GRCh38#46545944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91598630-A-C

46545944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91598630-A-T

46547383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91597948-G-T

http://identifiers.org/hco/11/GRCh38#46547384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91597947-C-A

46547384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91597947-C-T

46547413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91597910-T-A

46547413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91597910-T-C

46547413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91597910-T-G

46548099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91597185-A-G

46548183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91597102-T-C

46548183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91597102-T-G

46548537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91596752-T-C

46548537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91596752-T-G

http://identifiers.org/hco/11/GRCh38#46548542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91596747-C-A

46548542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91596747-C-T

46548571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91596718-T-A

http://identifiers.org/hco/11/GRCh38#46554425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91592808-A-C

46554438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91592795-A-T

46555539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91590404-G-A

46555540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91590403-G-T

46555697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91590265-T-C

46556349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91587592-G-A

46556367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91587574-A-G

46556443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91587495-T-G

46560444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91581474-A-G

46560715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91581108-T-C

http://identifiers.org/hco/11/GRCh38#46560874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91580931-C-A

46561040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91580770-C-T

46564901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91576660-A-G

46570964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91574538-A-G

46576998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91571370-C-T

46577119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91571251-G-A

46577620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91570852-G-A

46577679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91570809-G-A

46577738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91570752-G-C

46589477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91565025-G-A

46589990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91564451-A-G

46590872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

46590893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/11/GRCh38#46590894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/11/GRCh38#46590910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

46590940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

46590940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

46593321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91561196-C-T

46593526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91560999-A-T

46593558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91560992-C-G

46593787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91560763-A-G

46593787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91560763-A-T

46593855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91560695-C-G

46593855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91560695-C-T

http://identifiers.org/hco/11/GRCh38#46594009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25990
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#91560539-A-C