86288121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3 prime UTR variant
orthologous variants: 59920084-G-T

86288193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3 prime UTR variant
orthologous variants: 59920155-A-G

86288232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3 prime UTR variant
orthologous variants: 59920193-T-C

86288697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59920626-T-G

86288780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59920704-G-A

86288780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59920704-G-T

86288919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59920840-A-T

86288966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59920890-C-T

86288971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59920895-G-C

86296936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59922340-G-C

86297308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59922722-G-A

86298323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59926123-G-A

86298529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59926335-G-A

86298902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59926694-A-G

86299385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59927126-T-C

86300797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59929409-T-G

86301224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59929784-G-C

86301224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59929784-G-T

86301325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59929881-T-C

86301418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59929974-G-A

86301671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59930225-A-G

86301721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59930256-T-C

http://identifiers.org/hco/9/GRCh38#86301734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59930268-A-C

86301874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59930800-C-T

86303034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932529-T-C

86303034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932529-T-G

86303037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932532-G-A

86303037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932532-G-T

http://identifiers.org/hco/9/GRCh38#86303075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59932568-C-A

86303076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932569-A-G

86303076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932569-A-T

86303204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59932697-A-G

86303242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932730-T-A

86303250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932738-G-A

86303250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59932738-G-T

86303648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933065-T-A

86303849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933169-T-C

86303966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933272-T-G

86304057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933345-G-A

86304140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933421-T-C

86304154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933435-T-A

86304837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933514-G-A

86304837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933514-G-T

http://identifiers.org/hco/9/GRCh38#86304843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59933520-C-A

86305223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59933740-A-G

86305314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59933834-A-G

86305651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59934086-T-C

86306081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59934409-T-C

86306176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59934501-C-G

86308277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936109-G-T

http://identifiers.org/hco/9/GRCh38#86308278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59936110-C-A

86308508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59936353-T-C

86308570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59936415-A-G

86308635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936482-A-G

http://identifiers.org/hco/9/GRCh38#86308667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59936513-C-A

86308839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936688-G-A

86308995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936828-T-C

86309144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936930-A-G

86309154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936940-T-C

86309190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59936976-T-C

http://identifiers.org/hco/9/GRCh38#86310826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59939709-A-C

86310826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939709-A-G

86310901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939746-C-T

86310921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939765-T-C

86310939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939783-G-T

86311109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939933-G-A

86311109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59939933-G-T

86311349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59940135-A-G

86313369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59940403-G-A

86313446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59940431-C-T

86317301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59942339-C-T

http://identifiers.org/hco/9/GRCh38#86317613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59943030-C-A

86317613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943030-C-G

86317613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943030-C-T

86318000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943496-A-G

86318307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943752-T-C

86318342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943786-T-C

86318344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943788-T-G

86318401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59943891-G-A

86318445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59944008-T-A

86319509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59945425-G-A

86319509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59945425-G-T

86319628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 59945528-T-C

86319676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59945576-T-C

86320455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59946381-T-A

86322502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59946989-A-G

http://identifiers.org/hco/9/GRCh38#86322775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59947359-C-A

86322775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59947359-C-T

86322777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59947363-A-G

86322814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59947415-A-G

86322814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59947415-A-T

86322842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59947442-T-C

86322915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59947497-A-G

http://identifiers.org/hco/9/GRCh38#86322935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59947517-A-C

86322953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59947532-C-T

86322955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59947534-T-C

86322986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59947565-C-T

86323050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59947629-G-A

86323050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59947629-G-T

86323194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59947767-T-C

86323194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59947767-T-G

86323422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: synonymous variant
orthologous variants: 59947983-G-A

86323529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59948102-C-G

86323529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59948102-C-T

86323555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: missense variant
orthologous variants: 59948128-T-G

86323667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59948240-G-A

http://identifiers.org/hco/9/GRCh38#86323723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59948290-A-C

86323980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948551-G-A

86323980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948551-G-C

86324132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948707-T-A

86324288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948831-T-A

86324288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948831-T-C

86324288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948831-T-G

http://identifiers.org/hco/9/GRCh38#86324291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59948834-C-A

86324291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59948834-C-T

http://identifiers.org/hco/9/GRCh38#86324744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59949299-C-A

86324744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59949299-C-T

86324912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59949452-G-T

86325341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59949837-G-A

http://identifiers.org/hco/9/GRCh38#86325535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59950028-C-A

86325553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950046-T-C

86325849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950332-C-T

86325875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950344-G-A

86326264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950700-G-C

86326264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950700-G-T

86326361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59950796-C-T

http://identifiers.org/hco/9/GRCh38#86326599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59951024-C-A

86327477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59951823-C-T

86328439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59953136-T-G

http://identifiers.org/hco/9/GRCh38#86337165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59955662-C-A

86337234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59955717-G-A

86337234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59955717-G-T

86337282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59955760-T-C

86337300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59955765-G-T

86337315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59955778-T-C

86337443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 59955884-A-G

86338158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956199-A-G

86338244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956284-C-T

86338309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956343-T-C

http://identifiers.org/hco/9/GRCh38#86338311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59956345-A-C

86338315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956349-G-A

86338315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956349-G-C

86338338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956389-A-G

86338595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59956611-T-G

http://identifiers.org/hco/9/GRCh38#86338819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59957188-C-A

86338819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957188-C-G

86338819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957188-C-T

http://identifiers.org/hco/9/GRCh38#86339003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59957366-A-C

86339009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957372-C-G

86339101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957437-T-C

86339105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957441-T-C

86339128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957449-A-G

86339736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59957981-G-A

86340123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958471-A-G

86340147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958495-G-A

86340147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958495-G-T

86340178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958525-C-T

86340219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958550-C-G

http://identifiers.org/hco/9/GRCh38#86340221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59958552-A-C

86340221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958552-A-G

86340261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958591-A-G

86340523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958865-T-C

86340574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958909-A-G

86340574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59958909-A-T

http://identifiers.org/hco/9/GRCh38#86340898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59959220-A-C

86340898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59959220-A-G

86340945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59959264-G-T

86341164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59959491-T-G

86341858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59960292-T-G

86341931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59960359-G-A

86342806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59961698-C-G

86342937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59961826-G-A

86342937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59961826-G-T

86342945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59961834-A-G

86343061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59962666-C-T

86343108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59962713-C-T

http://identifiers.org/hco/9/GRCh38#86343244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59962846-A-C

86343244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59962846-A-G

http://identifiers.org/hco/9/GRCh38#86343267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59962869-C-A

86343267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59962869-C-T

86343537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963071-A-G

86345116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59963499-T-C

86345116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59963499-T-G

86345179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963560-A-T

86345277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963650-G-A

86345277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963650-G-T

http://identifiers.org/hco/9/GRCh38#86345286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59963659-C-A

86345450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963797-T-C

86345548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963908-A-T

86345577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59963949-A-G

86345639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59964030-G-A

86345732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59964148-T-C

86345732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59964148-T-G

86345882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59964273-T-C

86346176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59964367-G-A

86346176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59964367-G-T

86346900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965099-C-G

86346913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965112-C-T

86346925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965126-C-T

86346930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965131-T-C

86347026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965229-T-A

86347148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965329-T-A

86347247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965404-C-T

86347277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965431-G-A

86347359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965505-T-A

86347470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965807-C-T

86347495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59965830-A-G

86350652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59968226-G-T

86351930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59968587-G-A

86352092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59968799-C-G

http://identifiers.org/hco/9/GRCh38#86352421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59969138-C-A

86352421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59969138-C-T

86352507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59969257-T-C

http://identifiers.org/hco/9/GRCh38#86352523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59969269-C-A

86352523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59969269-C-T

86352524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59969270-T-C

86352894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59969588-C-G

86352894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59969588-C-T

86352903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59969597-C-G

86353034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59969728-T-A

86353034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59969728-T-C

86353044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59969738-T-C

86353155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59969849-G-A

86353155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 59969849-G-C

86353244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59969938-T-C

http://identifiers.org/hco/9/GRCh38#86353365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#59970049-C-A

86353365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: intron variant
orthologous variants: 59970049-C-G

86353507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59970161-T-C

86354248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59970767-G-A

86354248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 59970767-G-T

86354298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 59970815-T-C

http://identifiers.org/hco/9/GRCh38#86354415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#59970929-C-A

86354415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59970929-C-T

86354422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59970936-G-A

86354422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59970936-G-C

86354422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25817
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59970936-G-T