75469322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: non coding transcript exon variant
orthologous variants: 82095239-C-G

75469345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: non coding transcript exon variant
orthologous variants: 82095217-A-T

75469419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82095147-G-T

75469630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093991-C-T

http://identifiers.org/hco/2/GRCh38#75469660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82093963-A-C

75474019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093436-G-A

http://identifiers.org/hco/2/GRCh38#75474306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82093211-C-A

http://identifiers.org/hco/2/GRCh38#75474309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82093208-A-C

75474309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093208-A-T

75474311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093206-A-G

75474311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093206-A-T

75474436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82093129-C-G

http://identifiers.org/hco/2/GRCh38#75474454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82093104-C-A

75474457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82093101-G-A

75474498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82093060-G-T

75474502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82093056-A-T

http://identifiers.org/hco/2/GRCh38#75474535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82093023-C-A

75474535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82093023-C-T

75474547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82093006-C-T

75474567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82092986-A-G

75474621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82092924-A-G

http://identifiers.org/hco/2/GRCh38#75474973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82092602-A-C

http://identifiers.org/hco/2/GRCh38#75474986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82092589-C-A

75475131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092432-G-A

75475189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092374-C-T

http://identifiers.org/hco/2/GRCh38#75475284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82092229-C-A

75475301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092212-G-C

75475315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092198-G-A

75475315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092198-G-C

75475315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092198-G-T

75475337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092176-T-G

75475421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82092104-T-C

75476016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82091321-C-T

75476077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82091252-T-C

75476211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82091040-T-G

75476246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82090987-C-T

75476253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82090980-A-T

http://identifiers.org/hco/2/GRCh38#75476289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82090948-C-A

75476720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82089967-A-G

http://identifiers.org/hco/2/GRCh38#75476758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82089919-C-A

75476848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82089860-C-T

75477031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82089690-A-T

75477070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82089628-T-G

75481299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82088641-G-A

75481508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82087941-A-G

75481522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82087927-C-G

http://identifiers.org/hco/2/GRCh38#75482488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82086580-C-A

75482501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82086567-G-A

75482501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82086567-G-T

75482509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82086559-G-A

75482509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82086559-G-C

75482570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82086492-T-C

75482589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82086473-G-A

75482742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82086315-G-A

75482873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82085212-G-T

http://identifiers.org/hco/2/GRCh38#75482936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82085151-C-A

75482978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82085120-G-A

75483028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82085080-T-A

75483028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82085080-T-G

75483270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82084835-T-C

75483441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82084671-G-T

75483522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82083753-A-G

75483663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82083627-T-A

75483689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82083601-G-T

75483789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82083508-G-A

75483860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82083439-T-C

75484225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82082636-C-T

75484226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82082635-A-G

http://identifiers.org/hco/2/GRCh38#75484230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82082631-C-A

75484486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82082185-T-G

75484541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82082133-A-G

75484659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82082012-A-G

http://identifiers.org/hco/2/GRCh38#75484813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82076618-C-A

75484851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82076580-G-T

75485012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82076450-A-G

75485082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82076374-A-G

75485838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82075515-A-G

75486092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82075265-C-T

75487351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82073654-C-G

75487421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82073585-T-C

75487502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82073508-A-G

75491014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071525-G-A

75491149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071394-C-G

75491173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071371-G-A

75491252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071300-A-G

75491359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071181-T-C

75491538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82071001-C-T

75491563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82070977-A-G

75491592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82070948-G-C

75491739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82070811-G-T

75491826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82070733-A-T

75491915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82070645-C-T

75492076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82070327-T-C

75492174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82070214-T-C

75492270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82070127-G-A

75492360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82070037-T-G

75492375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82070022-T-A

http://identifiers.org/hco/2/GRCh38#75492444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069959-C-A

http://identifiers.org/hco/2/GRCh38#75492460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069943-C-A

75492811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069600-A-G

75492889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069520-T-G

75492940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069470-T-C

http://identifiers.org/hco/2/GRCh38#75492986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069437-A-C

75492986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069437-A-T

http://identifiers.org/hco/2/GRCh38#75493007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069415-C-A

http://identifiers.org/hco/2/GRCh38#75493020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069402-A-C

75493089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069288-T-C

75493109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069271-G-A

75493109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069271-G-T

75493117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069264-T-G

http://identifiers.org/hco/2/GRCh38#75493171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069213-C-A

75493171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069213-C-T

http://identifiers.org/hco/2/GRCh38#75493197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069182-C-A

http://identifiers.org/hco/2/GRCh38#75493206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82069173-C-A

75493206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82069173-C-G

75493243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 82069136-T-A

75493243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 82069136-T-C

75493330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 82069049-T-C

http://identifiers.org/hco/2/GRCh38#75493420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82068959-A-C

75493420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 82068959-A-G

http://identifiers.org/hco/2/GRCh38#75493570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82068812-A-C

75493570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 82068812-A-G

75493617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82068765-A-G

75493657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82068729-A-G

http://identifiers.org/hco/2/GRCh38#75493665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82068722-A-C

http://identifiers.org/hco/2/GRCh38#75493697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82068694-C-A

75493697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82068694-C-G

75493697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82068694-C-T

75494891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82066954-G-C

75499294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065750-G-A

75499341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065707-T-A

75499390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065648-T-G

http://identifiers.org/hco/2/GRCh38#75499495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82065543-A-C

75499638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065394-G-C

75499677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065355-A-G

75499764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065267-G-T

75499780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065241-G-A

75499855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065173-G-A

75499855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065173-G-C

75499861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065166-G-A

75499881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82065145-T-C

75502530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82062455-T-C

http://identifiers.org/hco/2/GRCh38#75502615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82062362-A-C

http://identifiers.org/hco/2/GRCh38#75502666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82062217-C-A

75503061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82061754-C-T

75503067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82061748-T-C

75503067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82061748-T-G

75503280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82061542-G-A

75503583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061244-G-T

75503584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061243-T-C

75503629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061198-C-G

75503632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061195-A-G

75504465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061045-C-G

75504465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82061045-C-T

75504537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82060973-C-T

75504605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82060906-C-G

75505039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82060822-T-C

75505054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82060806-T-C

http://identifiers.org/hco/2/GRCh38#75510872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82056694-C-A

75510921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056645-T-C

75510941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056624-T-C

75510984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056583-T-C

75511064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056509-A-G

75511161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056226-C-T

75511189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056195-T-C

http://identifiers.org/hco/2/GRCh38#75511292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82056096-A-C

75511381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82056023-C-T

75511430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82055991-T-C

75511447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82055980-G-T

75511569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82055869-G-C

75511949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82055747-G-A

75511954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82055742-G-C

http://identifiers.org/hco/2/GRCh38#75514544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82053922-A-C

75514585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82053864-C-T

75514652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82053791-G-A

75514746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82053700-T-C

75514819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82053627-T-C

75515359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82052999-A-G

http://identifiers.org/hco/2/GRCh38#75515525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82052893-C-A

75515525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82052893-C-T

http://identifiers.org/hco/2/GRCh38#75515539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82052879-A-C

75516021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82052445-G-A

75516743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82050075-C-T

75516812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82050006-T-G

75517510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048722-A-G

http://identifiers.org/hco/2/GRCh38#75517537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048695-C-A

75517546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048687-G-C

75517547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048686-A-G

75517668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048580-C-G

75517668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048580-C-T

http://identifiers.org/hco/2/GRCh38#75517670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048578-C-A

http://identifiers.org/hco/2/GRCh38#75517672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048576-C-A

75517672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048576-C-G

75517672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048576-C-T

75517684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048564-C-T

http://identifiers.org/hco/2/GRCh38#75517743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048498-C-A

75517743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048498-C-T

http://identifiers.org/hco/2/GRCh38#75517898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048360-C-A

75517898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82048360-C-G

75517948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82048320-T-G

75517951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82048317-G-A

75517951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82048317-G-T

75517968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82048293-A-T

http://identifiers.org/hco/2/GRCh38#75517999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048270-C-A

75517999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048270-C-G

75517999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048270-C-T

http://identifiers.org/hco/2/GRCh38#75518012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82048262-A-C

75518129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82048133-G-A

75518129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82048133-G-T

75518167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82048097-G-A

75518167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82048097-G-C

75518167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82048097-G-T

75518188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82048077-G-A

75518188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82048077-G-T

75518213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82048029-T-C

75518216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82048026-G-A

75518241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82048003-C-T

75518390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047961-T-C

http://identifiers.org/hco/2/GRCh38#75518495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82047912-C-A

75518495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047912-C-T

75518558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047851-C-T

75518567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047842-T-A

75518567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047842-T-C

75518593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047832-T-C

http://identifiers.org/hco/2/GRCh38#75518619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82047823-C-A

75518646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82047796-C-T

75518673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82047769-G-C

75518673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 82047769-G-T

75518778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047712-G-A

75518778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047712-G-T

75518797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82047693-T-C

75518865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047606-G-A

75518865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047606-G-C

75518865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047606-G-T

75518920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047552-T-C

75518920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047552-T-G

75519534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047136-G-C

75519584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047086-C-T

75519625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047017-C-T

75519626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82047016-G-A

75519693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046948-C-G

75519696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046945-T-G

75519740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046889-G-A

75519964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046726-T-C

http://identifiers.org/hco/2/GRCh38#75520106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82046613-C-A

75520199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046523-C-T

75520200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82046522-A-G

http://identifiers.org/hco/2/GRCh38#75522361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82044553-C-A

75522361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82044553-C-G

75522389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82044525-G-A

75522389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82044525-G-T

75522407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82044514-A-T

http://identifiers.org/hco/2/GRCh38#75522440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82044481-C-A

75522440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82044481-C-T

75522494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82044428-G-A

75523754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82040167-T-C

http://identifiers.org/hco/2/GRCh38#75525559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82038921-A-C

75525559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038921-A-T

75525723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038748-G-A

75525785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038688-G-A

75526009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038470-A-T

75526087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038445-G-A

75526087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038445-G-C

75526087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038445-G-T

http://identifiers.org/hco/2/GRCh38#75526112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82038434-C-A

75526297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038268-A-G

75526546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038096-T-C

75526632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82038025-G-A

75540454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036994-G-A

75540637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036811-G-A

75540637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036811-G-T

http://identifiers.org/hco/2/GRCh38#75540639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82036809-C-A

75540839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82036615-A-G

75540839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82036615-A-T

75540863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82036590-A-G

75541152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036430-A-G

75541152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036430-A-T

75541163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82036419-C-G

75543045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82034833-G-A

75543089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82034794-A-G

75543140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82034755-T-A

75543141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82034754-G-A

75543775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82033808-A-G

75543795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82033788-G-A

75543836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82033750-C-T

75543839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82033747-G-A

75544460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82032074-C-T

75544497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82032026-G-C

75544505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82032016-G-A

75544521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82032000-T-C

75544649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82031873-C-T

75549430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82030484-C-G

75549777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82030022-T-G

75550363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82029490-C-T

75550383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82029470-C-T

75550520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82029362-C-T

75550768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82029111-A-G

75551348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82028360-C-G

75551348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82028360-C-T

75551570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82028167-A-G

75551604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82028134-G-C

75552522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82027274-A-G

75552672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82027157-C-T

75552787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82027065-G-C

75552953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82026901-C-T

75553332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82026274-G-A

75553586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82026024-G-A

75554054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82025345-C-T

75554078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82025301-G-T

75554122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82025256-C-T

75554236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82025175-G-T

75554298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82025113-C-T

http://identifiers.org/hco/2/GRCh38#75554480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82024971-A-C

75554488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82024963-C-T

75554492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82024959-G-A

75554500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82024951-C-G

75554893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023794-T-C

75554916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023766-T-C

75554971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023720-G-C

75554971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023720-G-T

75555350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023433-T-A

75555350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023433-T-C

75555396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023391-A-G

75555774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82023005-T-C

75555845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82022933-G-A

75555890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82022896-G-A

75556421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82022575-T-G

75557061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82022259-C-T

75557171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82022163-A-G

http://identifiers.org/hco/2/GRCh38#75557221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82022107-A-C

75557448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021881-C-T

http://identifiers.org/hco/2/GRCh38#75557701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82021748-C-A

75557701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021748-C-T

75557842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021623-G-A

75558026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021439-A-G

75558055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021410-G-T

75558211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021299-C-T

75558270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82021243-G-A

75558488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82021026-G-A

75558573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82020990-G-A

http://identifiers.org/hco/2/GRCh38#75558584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82020979-C-A

75558825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82020736-A-G

75558960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82020633-G-C

75558966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82020627-G-C

75558998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82020595-A-G

75559063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82020537-G-C

http://identifiers.org/hco/2/GRCh38#75559181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82020450-A-C

75559533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019928-G-A

75559599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019869-G-A

75559600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019868-A-G

75559962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019512-C-G

75560242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019256-C-T

75560304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019200-G-A

75560377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019115-T-A

75560394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019105-C-G

75560422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82019074-T-C

75560547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018984-G-A

75560547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018984-G-T

75560739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82018841-C-T

75560768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018807-G-T

http://identifiers.org/hco/2/GRCh38#75560773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018802-C-A

75560773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018802-C-T

75560782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018793-G-A

75560782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018793-G-T

http://identifiers.org/hco/2/GRCh38#75560808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018765-C-A

75560810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018763-G-A

75560810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018763-G-T

75560865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018711-G-C

75560865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018711-G-T

75560872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018704-G-A

75560872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018704-G-T

75560882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018694-T-C

http://identifiers.org/hco/2/GRCh38#75560971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018617-C-A

75560971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018617-C-T

http://identifiers.org/hco/2/GRCh38#75560981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018605-C-A

75560981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018605-C-T

http://identifiers.org/hco/2/GRCh38#75560983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018603-C-A

75561123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018485-T-C

75561164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018444-A-G

http://identifiers.org/hco/2/GRCh38#75561221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#82018387-C-A

75561221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018387-C-T

75561279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018327-A-T

75561305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018297-G-T

75561315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018287-T-A

75561315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018287-T-C

75561428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82018179-A-T

75561618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018004-A-G

75561618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82018004-A-T

75562122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017661-T-A

75562135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017651-T-C

75562219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017588-T-C

75562319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017499-G-A

75562722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017119-C-G

75562777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82017070-T-C

75563251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82016651-C-G

75563259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82016633-C-T

http://identifiers.org/hco/2/GRCh38#75564881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82015922-C-A

75564881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82015922-C-T

http://identifiers.org/hco/2/GRCh38#75565051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82015772-A-C

75565051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82015772-A-G

75565179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82015644-C-T

http://identifiers.org/hco/2/GRCh38#75565840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#82014226-A-C

75565840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82014226-A-G

75565889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82014176-T-C

75567761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009898-C-T

75567841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009821-T-C

75567844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25816
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009818-G-A