http://identifiers.org/hco/22/GRCh38#24952805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113369046-C-A

24952805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113369046-C-G

24952805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113369046-C-T

24952916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113368967-T-A

24952932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113368947-C-G

24954185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113368557-C-T

24954726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113368154-C-G

24954732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113368148-C-G

24956559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113367241-G-A

24956559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113367241-G-C

24961335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113366053-T-A

24961363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113366025-A-G

24961447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113365944-G-C

24967201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364369-G-T

24967248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364320-T-C

24967348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364245-C-T

24967459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364168-G-A

24967459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364168-G-T

24967571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113364078-C-T

24968089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113363874-A-G

24968199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, undefined
orthologous variants: 113363777-G-C

24968351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, undefined
orthologous variants: 113363630-C-T

24970360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, undefined
orthologous variants: 113362353-G-T

24970490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113362224-G-A

24970502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113362213-A-G

24982474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113360513-A-G

24982701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113360309-C-T

24982870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113360190-C-T

24983076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113360043-T-C

24989527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113357268-C-T

24990902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113356017-A-G

24990928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113355993-C-T

25013209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347773-G-A

25013209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347773-G-T

25013212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347770-C-G

25013248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347740-G-T

http://identifiers.org/hco/22/GRCh38#25013265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113347725-C-A

25013265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347725-C-T

http://identifiers.org/hco/22/GRCh38#25013301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113347704-C-A

25013301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347704-C-G

25013310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347695-G-A

25013376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347651-G-T

25013484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347548-G-A

25013494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347538-C-G

http://identifiers.org/hco/22/GRCh38#25013575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113347468-C-A

25013629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347426-G-T

25013659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347401-G-A

http://identifiers.org/hco/22/GRCh38#25013679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113347381-C-A

25013743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347326-T-A

25013743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347326-T-G

25013823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347252-T-C

25013834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347241-A-G

http://identifiers.org/hco/22/GRCh38#25013867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113347215-C-A

25013867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347215-C-T

25014019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113347071-T-C

25015367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113345619-C-T

25022150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113344087-A-T

25022333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113343926-T-G

25023495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343516-A-G

25023513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343499-A-G

25024181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343221-T-C

25024187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343215-C-T

25024252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343151-T-C

25024274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113343135-T-C

http://identifiers.org/hco/22/GRCh38#25024322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113343099-C-A

25024604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113342910-T-C

25024692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342838-T-C

25024735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342799-A-G

25024746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342788-G-T

25024813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342758-T-A

25024813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342758-T-C

25024913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342678-G-A

25024976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342616-G-A

25025018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342575-G-A

25025081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342513-G-A

25025081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342513-G-T

http://identifiers.org/hco/22/GRCh38#25025095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113342499-C-A

25025095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342499-C-T

http://identifiers.org/hco/22/GRCh38#25025159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113342341-A-C

25025162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342338-G-C

http://identifiers.org/hco/22/GRCh38#25025245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113342246-C-A

25025322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113342137-G-A

25025442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341945-G-A

25025522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341875-C-T

25025524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341873-A-G

25025741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 113341669-T-C

http://identifiers.org/hco/22/GRCh38#25025761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113341648-C-A

25025775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 113341634-G-A

25025839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341587-G-T

25025859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341579-G-C

25025859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341579-G-T

25026375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113341132-G-A

25026891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113340776-G-T

25026933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113340746-C-T

http://identifiers.org/hco/22/GRCh38#25027760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113340235-A-C

http://identifiers.org/hco/22/GRCh38#25027859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113340155-C-A

25027859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113340155-C-G

25028238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339773-C-T

25028258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339753-A-T

25028349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339662-A-G

25028349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339662-A-T

25028374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113339637-G-A

http://identifiers.org/hco/22/GRCh38#25028411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113339600-C-A

25028411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339600-C-T

http://identifiers.org/hco/22/GRCh38#25028475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113339536-C-A

25028475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339536-C-T

25028567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, undefined
orthologous variants: 113339429-G-A

25028567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, undefined
orthologous variants: 113339429-G-C

http://identifiers.org/hco/22/GRCh38#25028604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113339392-A-C

25028711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous_variant, undefined
orthologous variants: 113339285-C-T

25028735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, undefined
orthologous variants: 113339261-A-G

25028735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, undefined
orthologous variants: 113339261-A-T

25028750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339246-A-G

http://identifiers.org/hco/22/GRCh38#25028771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113339225-C-A

25028771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339225-C-T

25028813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339183-C-T

http://identifiers.org/hco/22/GRCh38#25028850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113339146-C-A

25028850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339146-C-T

25028864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339132-G-C

25028864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113339132-G-T

25028884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113339112-G-A

25028956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113339049-C-T

http://identifiers.org/hco/22/GRCh38#25029017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113338988-C-A

25029038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338967-G-A

25029038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338967-G-T

25029071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338934-A-G

25029122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338889-T-A

25029129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338882-T-C

25029275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338736-G-A

25029326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113338685-C-T

25029347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338661-T-G

http://identifiers.org/hco/22/GRCh38#25029459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113338549-C-A

25029459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338549-C-G

25029459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113338549-C-T

25029523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113338485-G-A

http://identifiers.org/hco/22/GRCh38#25029600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113338404-C-A

25029600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113338404-C-T

25029694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113338331-A-G

http://identifiers.org/hco/22/GRCh38#25029908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113338178-A-C

25029928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113338157-A-G

25030773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113337246-C-T

25032458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336418-A-G

25032458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336418-A-T

25032459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336417-G-A

25032459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336417-G-T

25032485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336398-T-G

http://identifiers.org/hco/22/GRCh38#25032508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113336375-C-A

25032508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336375-C-T

25032513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336370-C-G

25032513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113336370-C-T

http://identifiers.org/hco/22/GRCh38#25038736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113332605-C-A

25038896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332445-G-A

25038901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332440-G-A

25038901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332440-G-T

25039014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113332327-G-A

25039014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113332327-G-C

25039030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332311-A-T

25039046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332295-A-T

25039047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113332294-C-T

25039048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332293-A-G

25039202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332148-A-G

25039255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113332095-G-A

25039255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: stop gained
orthologous variants: 113332095-G-T

http://identifiers.org/hco/22/GRCh38#25039393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113331960-A-C

25039393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331960-A-G

25039491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: synonymous variant
orthologous variants: 113331862-A-G

25039491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331862-A-T

http://identifiers.org/hco/22/GRCh38#25039519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113331834-A-C

25039519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331834-A-G

25039615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331714-A-G

25039615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331714-A-T

25039630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331702-A-G

http://identifiers.org/hco/22/GRCh38#25039789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113331633-C-A

25039789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331633-C-T

25039852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331570-G-A

25039939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331486-G-T

25039948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331477-A-G

http://identifiers.org/hco/22/GRCh38#25039954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113331471-C-A

25039996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331429-G-A

25039996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331429-G-C

25040013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331412-C-G

25040375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331050-T-A

25040375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113331050-T-C

25040561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense variant
orthologous variants: 113330868-G-A

25040619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113330815-C-G

25040619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113330815-C-T

25040758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330676-G-C

25040857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330574-G-A

25040857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330574-G-T

25040885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330546-A-G

http://identifiers.org/hco/22/GRCh38#25040891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113330540-C-A

25040891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330540-C-T

25040921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330510-G-T

25040922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330509-T-G

http://identifiers.org/hco/22/GRCh38#25041077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113330357-C-A

25041077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330357-C-T

http://identifiers.org/hco/22/GRCh38#25041221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113330225-C-A

25041221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330225-C-G

25041265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330181-T-G

25041397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330049-T-A

25041397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330049-T-G

25041418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113330028-G-C

25041418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 113330028-G-T

25041460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113329983-G-A

25041481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113329962-A-G

25043345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113328769-C-T

http://identifiers.org/hco/22/GRCh38#25043692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113328497-A-C

25043692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113328497-A-G

25043956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113328199-A-G

25044063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113328078-T-C

25044244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113327936-C-T

http://identifiers.org/hco/22/GRCh38#25044376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113327808-C-A

25044430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113327741-G-A

25044528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113327680-T-G

25048470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113323716-G-A

25048516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113323668-C-T

25048833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323437-G-C

25048833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323437-G-T

http://identifiers.org/hco/22/GRCh38#25048900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113323391-A-C

25048900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323391-A-G

25048900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323391-A-T

http://identifiers.org/hco/22/GRCh38#25048910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113323381-A-C

25048910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323381-A-G

25048910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323381-A-T

http://identifiers.org/hco/22/GRCh38#25048915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113323376-C-A

25048950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323357-G-C

25048950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113323357-G-T

25049047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113323287-G-A

25049047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113323287-G-T

http://identifiers.org/hco/22/GRCh38#25049091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113323269-C-A

25049292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113323141-G-C

25049295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113323138-G-A

25049337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113323096-C-G

25049354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113323079-G-T

25050723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321857-G-C

25050760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321832-T-C

25050853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321745-T-C

25050901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321699-A-G

25050972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321610-C-G

25051016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321552-A-G

25051040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321526-G-A

25051056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321510-G-T

http://identifiers.org/hco/22/GRCh38#25051088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321476-C-A

25051088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321476-C-T

25051090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321474-G-T

http://identifiers.org/hco/22/GRCh38#25051095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321469-C-A

25051095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321469-C-T

http://identifiers.org/hco/22/GRCh38#25051097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321467-C-A

25051099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321465-G-A

http://identifiers.org/hco/22/GRCh38#25051102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321462-C-A

25051110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321458-G-A

25051110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321458-G-T

http://identifiers.org/hco/22/GRCh38#25051112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321456-C-A

25051138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321453-A-G

http://identifiers.org/hco/22/GRCh38#25051211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113321405-C-A

25051226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321390-G-A

25051226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113321390-G-T

25051247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 113321369-G-T

25065361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315078-G-T

25065372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315067-G-A

25065372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315067-G-T

25065383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315056-G-T

25065389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315050-G-T

25065400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113315030-C-T

25066816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113313789-T-G

25067267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113313687-T-A

25067267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113313687-T-C

25067375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113313525-C-T

25067873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312872-C-T

25067904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312854-C-T

25068072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312694-C-G

25068163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312596-C-T

25068287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312449-G-A

25068287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312449-G-C

25068333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312404-G-A

25068333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312404-G-T

25068336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113312401-G-A

http://identifiers.org/hco/22/GRCh38#25068357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113312381-C-A

25070150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113311188-G-A

25070150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113311188-G-T

25070199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113311142-G-A

25070199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113311142-G-T

25070203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113311138-T-G

25070354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113310985-T-A

25070354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113310985-T-C

25070356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113310983-G-A

25070356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113310983-G-C

25070356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113310983-G-T

25070450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310906-G-A

25070450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310906-G-C

25070450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310906-G-T

25070451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310905-G-A

25070451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310905-G-C

25070451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310905-G-T

25070507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310883-T-G

25070609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310792-A-G

25071245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310340-G-A

25071245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310340-G-C

25071245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113310340-G-T

25072354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113309321-G-C

25072721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113309034-C-T

25072722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113309033-G-A

25072738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113309017-G-A

25072846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113308916-T-A

25075101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113307924-A-G

25076274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113307044-G-A

25076400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306923-T-G

25076512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306812-A-G

25076782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306597-G-A

25076852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306527-G-A

25077030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306358-G-A

25077185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306229-G-A

25077206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306207-T-C

25077223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306190-G-C

25077364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113306091-C-T

25078077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113305430-G-A

25078152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113305357-C-G

25079103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113304812-G-A

http://identifiers.org/hco/22/GRCh38#25079433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113304628-A-C

25079433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113304628-A-T

25079515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113304548-G-C

25079853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113304292-A-G

25080529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113304012-T-C

25080769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113303882-G-A

25080866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113303797-G-A

25080898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113303765-G-A

25081165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113303573-T-C

http://identifiers.org/hco/22/GRCh38#25081312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113303452-A-C

25081424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113303398-T-C

25083635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113301556-C-T

25083766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113301406-T-C

http://identifiers.org/hco/22/GRCh38#25083951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113301244-C-A

25083958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113301237-A-G

25083960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113301235-G-C

http://identifiers.org/hco/22/GRCh38#25084046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113301165-C-A

25084071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113301141-G-A

http://identifiers.org/hco/22/GRCh38#25086067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113300093-A-C

25086113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113300054-G-A

25086514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113299707-G-A

25086656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113299603-A-G

25086698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113299561-G-C

http://identifiers.org/hco/22/GRCh38#25104283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113291433-C-A

http://identifiers.org/hco/22/GRCh38#25105522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113290654-C-A

25105707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113290487-G-A

25105894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113290385-G-A

25105894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113290385-G-T

25108201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113288634-A-G

25108365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113288476-A-G

25108506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113288366-T-C

25108749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113288115-T-C

25108881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113288001-G-C

25109007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113287898-C-T

25110219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113287521-T-C

25110415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113287323-C-T

http://identifiers.org/hco/22/GRCh38#25110520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113287226-C-A

25110764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113287095-A-G

25110805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113287055-G-A

25111052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113286811-A-G

25111071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113286788-A-G

25111960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113286032-A-T

http://identifiers.org/hco/22/GRCh38#25111971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113286021-C-A

http://identifiers.org/hco/22/GRCh38#25112114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113285907-A-C

25112202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113285826-A-G

http://identifiers.org/hco/22/GRCh38#25112277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113285751-A-C

25112305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113285726-G-T

25112397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113285634-G-A

25112397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113285634-G-T

http://identifiers.org/hco/22/GRCh38#25112424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113285607-C-A

25112424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, synonymous_variant, undefined
orthologous variants: 113285607-C-T

http://identifiers.org/hco/22/GRCh38#25112631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113285412-C-A

25112631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113285412-C-T

25112900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113285152-G-A

http://identifiers.org/hco/22/GRCh38#25113103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113284966-C-A

25113700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113284540-C-T

25113983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113284371-C-T

25114291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113284155-T-C

25114359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113284096-C-T

25114475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113284007-C-G

25114565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113283945-G-T

25114618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113283869-G-A

25114716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113283799-A-G

25114752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113283763-C-G

25120160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113281480-C-G

25120307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113281412-G-T

25120589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113281167-T-C

25120615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113281141-A-T

25120956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113280828-G-A

25121127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113280709-G-A

25123628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113279358-A-G

25123628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113279358-A-T

http://identifiers.org/hco/22/GRCh38#25123738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113279251-C-A

25125725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113277034-C-T

http://identifiers.org/hco/22/GRCh38#25126124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113276668-C-A

25126152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113276577-T-C

25126254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113276490-T-C

25126495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113276217-T-G

25126607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113276108-C-T

25127245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275659-C-T

25127313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275599-T-C

25127570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275371-C-T

25127677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275276-C-T

25127678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275275-G-A

25127828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275142-A-G

25127828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275142-A-T

25127948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275035-G-T

25127976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113275015-G-C

25131480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113270760-C-T

25133961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113269378-T-C

25134028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113269327-G-A

25134065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113269288-C-T

25135496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113268062-T-A

25135859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113267764-G-A

25135859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113267764-G-T

25137930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113267122-G-A

25138356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113266779-G-C

25138532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113266665-T-C

25145239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113262342-A-G

25145565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113262094-G-T

25167600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113251240-T-A

25169610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113250491-A-G

25169656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113250447-G-A

25169679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113250426-A-G

25170725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113249501-G-A

25170725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113249501-G-C

25170725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113249501-G-T

25170736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113249490-T-C

25170811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113249450-T-G

25172221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247715-G-A

25172221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247715-G-T

25172223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247713-G-A

25172223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247713-G-T

25172313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247636-C-G

25172313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113247636-C-T

25174090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245829-A-T

25174102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245817-G-A

25174102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245817-G-T

25174105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245814-G-T

http://identifiers.org/hco/22/GRCh38#25174175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245763-C-A

25174201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245739-C-T

25174202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245738-T-C

http://identifiers.org/hco/22/GRCh38#25174219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245720-C-A

25174219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113245720-C-T

25174247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113245695-A-G

25174277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113245659-A-T

25174351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113245597-G-T

25174384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113245564-C-T

25174400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113245548-A-G

25174494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245457-G-A

25174554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245405-A-G

25174558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245401-C-T

25174597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245362-T-A

http://identifiers.org/hco/22/GRCh38#25174681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245286-A-C

25174681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245286-A-G

25174687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245280-T-C

http://identifiers.org/hco/22/GRCh38#25174729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245242-C-A

25174729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245242-C-T

25174742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245231-A-G

25174793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245179-T-C

25174793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245179-T-G

25174880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245109-T-C

25174880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245109-T-G

25174887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245102-G-A

25174887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245102-G-T

http://identifiers.org/hco/22/GRCh38#25174913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245087-A-C

http://identifiers.org/hco/22/GRCh38#25174922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245078-C-A

http://identifiers.org/hco/22/GRCh38#25174995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113245046-C-A

25175000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113245041-G-T

http://identifiers.org/hco/22/GRCh38#25175063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244996-C-A

25175063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244996-C-G

25175068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244990-A-G

http://identifiers.org/hco/22/GRCh38#25175089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244963-C-A

25175100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244953-G-A

25175100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244953-G-T

25175115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244938-T-C

25175147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244905-T-C

http://identifiers.org/hco/22/GRCh38#25175168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244883-C-A

25175168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244883-C-G

25175183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244865-C-T

25175282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244737-T-C

25175283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244736-G-A

25175334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244663-C-T

25175460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244562-T-A

25175467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244555-G-A

25175470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244552-C-T

25175484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244540-G-T

http://identifiers.org/hco/22/GRCh38#25175486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244538-C-A

http://identifiers.org/hco/22/GRCh38#25175531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244501-C-A

http://identifiers.org/hco/22/GRCh38#25175631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244392-C-A

25175631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244392-C-G

25175631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244392-C-T

25175632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244391-C-T

http://identifiers.org/hco/22/GRCh38#25175665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244343-C-A

25175665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244343-C-T

25175688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244324-T-C

25175726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244276-C-T

http://identifiers.org/hco/22/GRCh38#25175740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244252-C-A

25175804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244189-A-G

25175827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244166-G-A

25175828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244165-T-C

25175869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244141-G-T

25175875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244135-G-A

25176798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244067-G-C

25176798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244067-G-T

25176813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244057-G-A

25176813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244057-G-C

25176813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244057-G-T

25176837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244028-C-G

25176837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244028-C-T

http://identifiers.org/hco/22/GRCh38#25176838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244027-C-A

25176838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244027-C-T

25176846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244019-T-C

http://identifiers.org/hco/22/GRCh38#25176859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113244006-C-A

25176859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113244006-C-T

http://identifiers.org/hco/22/GRCh38#25176925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243959-C-A

25176925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243959-C-T

http://identifiers.org/hco/22/GRCh38#25176992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243888-C-A

25176992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243888-C-T

25177028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243870-G-T

http://identifiers.org/hco/22/GRCh38#25177133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243806-C-A

25177133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243806-C-T

http://identifiers.org/hco/22/GRCh38#25177135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243804-C-A

25177135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243804-C-T

25177174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243790-G-A

25177174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243790-G-C

25177188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243775-T-C

http://identifiers.org/hco/22/GRCh38#25177225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243734-C-A

25177225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243734-C-T

25177229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243730-G-C

25177229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243730-G-T

http://identifiers.org/hco/22/GRCh38#25177235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243724-A-C

25177235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243724-A-T

25177242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243717-T-G

25177270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243693-T-C

25177301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243671-G-A

25177312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243660-T-C

25177312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113243660-T-G

25177387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113243589-G-C

25177412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113243564-G-A

25177412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113243564-G-T

25177432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113243544-T-C

25177453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113243523-A-G

25177467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113243509-C-T

25177497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113243479-C-T

http://identifiers.org/hco/22/GRCh38#25177563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243413-C-A

25177563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113243413-C-T

http://identifiers.org/hco/22/GRCh38#25177566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243410-C-A

25177602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113243374-C-G

25177602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113243374-C-T

25177604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113243372-G-A

25177604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113243372-G-T

http://identifiers.org/hco/22/GRCh38#25177624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113243361-A-C

http://identifiers.org/hco/22/GRCh38#25181619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113242007-C-A

25181637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113241994-G-T

25181662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113241981-G-T

25181663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113241980-C-T

25181707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241940-T-C

25181743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241910-G-A

25181743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241910-G-T

25181761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241892-A-G

25181761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241892-A-T

25181827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113241825-C-G

25184956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113241129-T-C

25185004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241081-G-T

25185016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241069-G-A

25185016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113241069-G-C

http://identifiers.org/hco/22/GRCh38#25185095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240990-C-A

25185095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113240990-C-T

25185135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240954-G-A

25185253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240831-T-C

25185269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240815-T-A

25185269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240815-T-G

http://identifiers.org/hco/22/GRCh38#25185294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240791-C-A

25185294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240791-C-G

25185294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240791-C-T

http://identifiers.org/hco/22/GRCh38#25185353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240743-C-A

25185353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240743-C-G

25185353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240743-C-T

25185382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240718-G-A

25185382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240718-G-T

http://identifiers.org/hco/22/GRCh38#25185457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240648-C-A

25185477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113240630-A-G

http://identifiers.org/hco/22/GRCh38#25185483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240624-A-C

http://identifiers.org/hco/22/GRCh38#25190836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240248-A-C

http://identifiers.org/hco/22/GRCh38#25190847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240243-A-C

25190847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113240243-A-G

http://identifiers.org/hco/22/GRCh38#25190882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113240230-C-A

25190882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113240230-C-T

25190887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113240225-G-T

25191106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: intron variant
orthologous variants: 113240109-G-T

25192534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238765-G-A

25192534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238765-G-T

25192663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238684-G-A

25192663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238684-G-T

http://identifiers.org/hco/22/GRCh38#25192729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113238619-C-A

25192731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238617-G-C

25192829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238569-C-T

25192846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238555-T-A

http://identifiers.org/hco/22/GRCh38#25192986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113238392-A-C

25192986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238392-A-T

25193025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238349-T-C

25193224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238171-T-C

25193315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238095-T-C

25193319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238091-G-A

25193319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238091-G-T

25193323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238087-T-A

25193323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113238087-T-C

25193522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237518-G-A

25193522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237518-G-T

25193539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237501-C-T

25193547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237493-G-T

25193612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237440-T-C

http://identifiers.org/hco/22/GRCh38#25193613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113237439-C-A

25193615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237437-T-C

http://identifiers.org/hco/22/GRCh38#25193634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113237430-C-A

25193696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237354-G-T

25193700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237350-A-G

25193700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113237350-A-T

25194367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236840-C-T

25194508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236720-C-T

25194592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236644-T-A

25194713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236542-G-T

http://identifiers.org/hco/22/GRCh38#25194714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236541-A-C

http://identifiers.org/hco/22/GRCh38#25194744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236524-A-C

25194744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236524-A-G

25194748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236520-C-G

25194753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236515-T-C

25194769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236501-A-G

http://identifiers.org/hco/22/GRCh38#25194961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236340-C-A

http://identifiers.org/hco/22/GRCh38#25195023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236311-C-A

http://identifiers.org/hco/22/GRCh38#25195052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236282-C-A

25195176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236191-C-T

25195288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113236105-C-T

http://identifiers.org/hco/22/GRCh38#25195388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113236022-C-A

25196762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113234789-T-C

25196866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113234697-A-G

25197030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113234576-T-C

25197105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113234524-A-G

25197261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29345
most severe consequence: 3 prime UTR variant
orthologous variants: 113234362-T-C