69573469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89597948-T-G

http://identifiers.org/hco/18/GRCh38#69573580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89597837-C-A

69573815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89597581-T-A

69576320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89596280-T-A

69576617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89596047-A-G

http://identifiers.org/hco/18/GRCh38#69576791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89595879-C-A

http://identifiers.org/hco/18/GRCh38#69577049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89595518-A-C

69577049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89595518-A-G

http://identifiers.org/hco/18/GRCh38#69577149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89595414-C-A

69577319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89595062-G-A

69577587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89594797-G-T

69577678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89594706-A-G

69578333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89594110-G-T

http://identifiers.org/hco/18/GRCh38#69578398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89594054-A-C

http://identifiers.org/hco/18/GRCh38#69578522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89593922-C-A

69578522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89593922-C-T

69578678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89593771-C-T

69586152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89592118-C-T

69586488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591812-T-C

69586693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591641-G-A

69586759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591576-G-A

69586759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591576-G-C

69586842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591493-G-C

69586963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591389-A-G

69587068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89591310-T-A

69588947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89589654-T-C

http://identifiers.org/hco/18/GRCh38#69589189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89589392-A-C

69589232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89589339-C-T

69589378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89589207-G-T

69589426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89589151-G-C

http://identifiers.org/hco/18/GRCh38#69589492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89589058-C-A

69589492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89589058-C-T

69590047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89588537-A-G

69590177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89588435-G-A

69590659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89586199-C-T

69590705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89586151-A-T

69590828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89586045-G-A

69590910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585964-G-C

69591061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585853-C-T

69591262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585519-C-G

69591301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585444-G-A

69591301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585444-G-C

69591352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585387-A-T

69591471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585260-G-A

69591707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585045-C-T

69591756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89585024-C-T

69593698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582549-T-C

69593843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582406-T-A

69594077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582156-A-T

69594107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582126-G-A

http://identifiers.org/hco/18/GRCh38#69594155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89582070-C-A

69594178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582047-G-A

69594178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89582047-G-T

69599095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578637-T-A

69599247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578489-G-A

69599247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578489-G-T

69599332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578399-A-G

69599332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578399-A-T

http://identifiers.org/hco/18/GRCh38#69599341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89578390-C-A

69599341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578390-C-T

69599347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89578384-T-C

http://identifiers.org/hco/18/GRCh38#69599630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89577990-C-A

69599642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577978-G-A

69599642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577978-G-T

69599723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577887-G-A

69600064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577562-G-A

69600175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577456-G-A

69600175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577456-G-C

69600196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577435-G-C

69600342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577310-C-G

69600674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577213-T-A

69600685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577201-T-C

69600709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89577182-A-G

69601059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89576850-A-G

69601238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89576095-A-G

69601386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89575945-C-T

69601557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89575787-A-G

69602056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89575310-T-C

69602133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89575255-T-C

http://identifiers.org/hco/18/GRCh38#69602145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89575243-C-A

69602412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89575013-T-C

69604004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574924-G-T

69604099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574830-T-C

69604217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574724-C-T

69604503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574467-G-C

69604512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574458-T-C

69604525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574444-A-T

69604566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89574396-A-G

69604779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89572448-A-G

69604821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89572405-T-G

69614653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89571174-A-G

69614804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89567857-C-T

69615081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89567567-T-C

69615308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89567263-G-A

69615539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89567037-T-C

69615883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566701-A-G

69615883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566701-A-T

69615944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566629-G-A

69616043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566592-C-T

69616286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566391-G-A

69616477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566284-T-A

69616549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566214-A-G

69616565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566198-T-C

69616734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89566103-T-G

69616854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89565982-A-G

69616874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89565962-C-T

69617061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89565784-C-T

69618964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564321-A-T

69619018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564278-A-G

http://identifiers.org/hco/18/GRCh38#69619050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89564220-C-A

69619143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564076-G-A

69619163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564056-T-C

69619220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564002-T-A

69619222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89564000-T-C

69619334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89563897-C-G

69619502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89563751-C-T

69619647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89563560-A-G

69619774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89563438-T-C

69619817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89563394-G-T

69621820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89561625-G-A

http://identifiers.org/hco/18/GRCh38#69621841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89561604-A-C

69621850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89561591-T-C

69621895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89561548-G-C

69622226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89560257-G-T

http://identifiers.org/hco/18/GRCh38#69622236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89560247-C-A

69622249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89560234-A-T

69622275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89560221-T-C

69622343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89560154-T-A

69622548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89560021-A-G

69622677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89559894-T-C

69622765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89559828-T-C

69622797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89559796-A-G

69623445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89558205-A-G

69623630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89558030-G-A

69623894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89557774-C-T

http://identifiers.org/hco/18/GRCh38#69624065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89557616-A-C

69624210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89557493-T-C

69624234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89557469-A-G

69624324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89557379-G-A

69624467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89557263-G-A

69625210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89556112-G-C

69625601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555726-G-A

http://identifiers.org/hco/18/GRCh38#69625736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89555596-C-A

69625736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555596-C-T

69625860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555493-A-G

69625991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555367-G-A

69625997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555361-A-T

69626009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555349-T-C

69626322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89555293-C-T

http://identifiers.org/hco/18/GRCh38#69626521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89555119-A-C

69626824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89554825-A-T

http://identifiers.org/hco/18/GRCh38#69626858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89554790-C-A

69626858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89554790-C-T

69627841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89554116-T-A

69627911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89554050-C-T

69628514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89553796-G-A

69628552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89553761-A-G

69628759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89553613-G-T

69628933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89552186-A-G

http://identifiers.org/hco/18/GRCh38#69629043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89552073-C-A

http://identifiers.org/hco/18/GRCh38#69629236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89551855-C-A

69629350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89551731-T-G

69629443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89551641-G-A

69629581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89551503-T-G

69630417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89550099-A-G

69630423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89550093-G-A

69630851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89549660-C-T

69630915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89549600-T-C

http://identifiers.org/hco/18/GRCh38#69631165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89549358-C-A

69631165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89549358-C-T

69631864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89548714-T-G

69632315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89548365-T-C

69632607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89545713-A-G

69632732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89545586-A-G

69636938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541413-A-G

69636996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541332-G-C

69637116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541240-C-T

http://identifiers.org/hco/18/GRCh38#69637129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89541217-C-A

69637205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541141-T-G

69637375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541005-G-A

69637375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89541005-G-T

http://identifiers.org/hco/18/GRCh38#69637781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89540594-C-A

69637834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89540534-A-T

69637901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89540477-C-G

69638061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89540320-C-G

69638081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89540301-T-G

69638174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89540223-A-G

http://identifiers.org/hco/18/GRCh38#69638286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89540095-A-C

69638397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539984-G-A

69638500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539853-G-T

69638560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539797-T-G

69639089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539070-T-C

69639111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539047-A-G

69639111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89539047-A-T

69639361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538635-A-G

69639411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538589-C-T

69639498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538516-T-C

69639503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538511-T-C

http://identifiers.org/hco/18/GRCh38#69639585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89538438-C-A

69639606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538413-G-A

69639970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538047-G-A

69639970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538047-G-C

69639994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89538022-G-A

69640075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89537931-T-C

69640232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89537707-C-T

69640245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89537689-A-G

69640339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89537587-G-A

69641359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89531947-T-C

69641571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89531751-C-T

69641670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89531665-T-A

69641765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89531604-C-T

69646426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89528629-G-A

69646555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89528484-G-A

69646606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89528433-G-A

http://identifiers.org/hco/18/GRCh38#69646644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89528415-C-A

69647012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89528141-T-G

http://identifiers.org/hco/18/GRCh38#69647402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89527933-A-C

69647493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89527896-A-T

69647501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89527888-A-G

69647583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527825-G-A

69647583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527825-G-T

69647601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527804-G-A

69647601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527804-G-C

69647648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527760-G-A

69647704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527703-G-T

69647859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527550-C-G

http://identifiers.org/hco/18/GRCh38#69648146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89527356-A-C

69648497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527252-C-G

69648499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527250-A-G

69648748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527029-G-A

69648748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89527029-G-T

69648809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89526975-T-C

69648849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89526952-T-C

69651975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89523199-C-G

69651975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89523199-C-T

69652119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89523042-T-A

69652119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89523042-T-C

69652334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89522872-T-C

69671388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89520257-T-C

69671699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89519934-C-T

69671927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89519703-G-C

69672011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89519647-G-C

69672801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89519392-A-G

http://identifiers.org/hco/18/GRCh38#69673034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89519193-C-A

69673034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89519193-C-T

http://identifiers.org/hco/18/GRCh38#69673655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89518665-C-A

http://identifiers.org/hco/18/GRCh38#69676199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89517035-C-A

69676199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89517035-C-T

69676212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89517022-G-A

69678044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89514815-T-C

69678397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89514523-G-C

69679233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89514043-A-G

69679233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89514043-A-T

69679277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89513998-T-C

69680044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89513270-G-C

69680601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89511798-A-T

69680837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89511549-T-C

69681213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89508988-A-G

69681295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89508909-C-T

69681380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89508813-T-G

69681393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89508802-G-A

69681507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89508687-G-T

69691591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89504905-A-G

69691597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89504899-A-G

69691721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89504740-G-A

69691859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89504613-C-T

69692262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89504306-T-A

http://identifiers.org/hco/18/GRCh38#69692577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89504050-A-C

69694284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89499553-G-A

69694284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89499553-G-T

http://identifiers.org/hco/18/GRCh38#69694384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89499424-C-A

69694747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89499132-T-C

69694863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89499013-A-T

69694953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498944-C-T

69695006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498891-G-C

69695007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498890-G-A

69695163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498750-C-T

69695299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498638-G-A

69695797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89498009-A-T

69696190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89497182-C-T

69696769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89496653-G-A

69697130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89496300-A-G

69697386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89496053-G-A

69697386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89496053-G-T

69697424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89496015-T-A

69697495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89495948-A-T

69697684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89495779-A-G

69698597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491971-A-G

69698638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491945-C-T

69698682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491903-T-C

69699073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491400-G-T

69699110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491363-C-G

69699131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491342-C-T

69699141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491332-C-G

69699257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491132-T-C

69699293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491096-T-C

69699336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89491052-T-A

69699517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89490888-C-T

69700593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89482426-T-C

69700746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89482326-G-A

69700746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89482326-G-T

69700789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89482283-C-T

69701056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481345-G-A

69701056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481345-G-T

69701124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481277-T-G

69701189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481210-A-G

69701219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481179-G-A

69701267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481141-C-G

69701324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89481080-T-G

69702458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89479993-T-C

69703051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89479440-G-A

69703234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89479303-T-C

69703504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89479062-A-G

69703799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478775-C-T

69703858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478735-T-C

69703882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478712-G-C

69703882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478712-G-T

69704247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478351-C-T

69704255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478343-G-A

69704255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478343-G-C

69704290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89478302-A-G

69708065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89475333-G-A

69708065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89475333-G-C

69708302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89475090-T-C

69708878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474830-T-C

69709038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474723-C-T

69709113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474634-A-G

69709167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474567-A-G

69709470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474296-T-C

69709598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89474164-C-G

69711591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89473850-T-C

69711632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89473809-T-C

69714259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89473157-T-C

69714280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89473136-T-C

69714408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89473022-G-A

69714502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472938-T-C

69714586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472861-T-C

69714598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472850-G-A

69714735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472723-G-A

69715056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472415-T-G

69715074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472397-C-T

69715131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472336-A-G

69715141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89472328-G-A

69715516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89471976-C-T

http://identifiers.org/hco/18/GRCh38#69715927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89471640-A-C

69715996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89471575-T-C

69716053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89471515-T-C

69716277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89471347-T-C

69716472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89471164-A-G

69716766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89470901-C-T

69716968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89470700-G-T

69721608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89459809-C-G

69722369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89459051-G-A

69722402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89459027-G-C

69722460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89458969-A-G

69722479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89458950-C-T

69722742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89456268-A-T

http://identifiers.org/hco/18/GRCh38#69722768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89456244-A-C

69722781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455818-A-T

http://identifiers.org/hco/18/GRCh38#69722891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89455711-C-A

http://identifiers.org/hco/18/GRCh38#69722925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89455681-A-C

69722966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455640-A-G

69723198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455407-G-A

69723251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455355-T-C

69723335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455282-G-C

69723461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455156-T-C

69723499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455123-G-A

69723513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455109-T-C

69723546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89455082-T-C

http://identifiers.org/hco/18/GRCh38#69723687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89450940-A-C

69723688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89450939-A-G

69723816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89450836-T-C

69723907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89450747-A-T

69724118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89450557-G-T

69724775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89449915-G-T

http://identifiers.org/hco/18/GRCh38#69724810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89449892-C-A

69724971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89449731-T-C

69724993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89449708-T-C

69725878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89449307-G-A

69725920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89449265-G-A

69725921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89449264-C-T

http://identifiers.org/hco/18/GRCh38#69725985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89449208-C-A

69726245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89448943-T-C

69726451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89448743-A-G

69727238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89448137-C-T

69727445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89447805-G-A

69727607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89447645-A-T

69727689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89447565-A-G

69734098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89445099-T-C

69734418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89444852-G-A

69734418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89444852-G-T

69734949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89443773-G-A

69734965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89443758-C-T

69735073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89443650-C-T

69735249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89443476-A-G

69736547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89441593-T-C

69736577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89441564-A-T

69736597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89441544-T-G

http://identifiers.org/hco/18/GRCh38#69737013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89441271-A-C

69738284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89440213-C-T

69738819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439362-G-A

69738819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439362-G-T

69738883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439319-G-C

69738883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439319-G-T

69738918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439284-C-G

69738918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439284-C-T

69738926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439276-C-T

69738928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89439274-T-A

69746648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89438603-C-T

69746790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89438463-C-G

69753591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89437156-A-T

69753668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89437090-C-T

69753907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89436889-T-C

69753946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89436847-T-A

69754722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89435789-A-G

69754953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89435584-G-A

69755477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89435145-G-C

69755544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89435077-G-A

69757612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89433216-A-T

http://identifiers.org/hco/18/GRCh38#69757681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89433141-C-A

69757727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89433097-G-A

69757780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89433043-A-G

69757930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432892-G-A

69757930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432892-G-T

69757955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432867-G-A

69758015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432802-C-T

69758202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432609-G-T

69758225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432583-T-C

69758334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432487-C-T

69758423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432428-G-A

69758455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432396-A-G

69758530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432333-T-C

69758546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432317-T-C

http://identifiers.org/hco/18/GRCh38#69758559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89432305-A-C

69758627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89432272-G-A

69759555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425367-T-C

69759581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425341-C-T

69759655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425266-A-G

69759987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424993-T-C

69759987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424993-T-G

69759997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424983-C-G

69760012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424964-T-C

69760165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424802-G-A

69760247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424720-T-C

69760279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424689-T-C

69760289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89424679-C-T

69762793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423751-C-T

69763058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423623-A-G

69763151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423552-A-G

69763173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423530-A-G

69763219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423489-G-A

69763219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89423489-G-C

69764765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89422246-T-C

69764874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89422153-T-G

69765058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89421947-T-C

69765078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89421927-T-C

69765128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89421878-A-G

69765136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89421872-T-C

69765357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89421528-T-G

69767379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420737-T-C

69767727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420464-T-C

69770246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419217-G-A

69770722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418785-T-A

69776274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89417903-C-T

69777986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411879-G-T

http://identifiers.org/hco/18/GRCh38#69778314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89411576-A-C

69778314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411576-A-T

69778582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411326-G-A

69778582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411326-G-T

69778608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411300-T-C

http://identifiers.org/hco/18/GRCh38#69778694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89411212-C-A

69778694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89411212-C-T

69778839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408528-T-C

69778839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408528-T-G

http://identifiers.org/hco/18/GRCh38#69779046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89408340-C-A

69779109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408270-G-A

69779124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408255-A-G

69779337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408081-C-G

69779360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89408060-C-T

69779819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89407905-A-G

69780070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89407656-A-G

69780978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89406729-G-A

69781153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89406570-G-A

69781225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89406503-A-G

69781352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89406370-T-C

69781356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89406366-T-A

69781468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89406254-T-C

http://identifiers.org/hco/18/GRCh38#69781500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89406221-C-A

69781500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89406221-C-T

69781562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89406172-C-T

http://identifiers.org/hco/18/GRCh38#69781570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89406164-C-A

69781570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89406164-C-T

69781709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89406014-T-A

69781896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89402906-T-C

69782060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: -T-G

69782862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89402052-T-G

69783123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89401824-C-T

69783298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89401676-T-C

69783849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89400769-T-C

http://identifiers.org/hco/18/GRCh38#69784424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89400259-A-C

69784613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89400116-G-T

69785058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89399668-C-T

69785204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89399526-G-T

69785401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89399330-A-G

69785610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89399127-C-T

69785655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89399089-T-C

69786067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89383724-C-T

http://identifiers.org/hco/18/GRCh38#69786404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89383326-C-A

69786511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89383187-G-A

69788189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89382558-T-C

69788258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89382493-G-T

69788439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89382344-A-G

69788464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89382320-T-C

69788794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89381978-A-G

69788992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89381801-G-C

69794009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89378480-T-A

69794009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89378480-T-C

69794235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89378248-A-G

69795885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89377345-G-A

69796397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89376853-A-G

69796460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89376785-G-C

http://identifiers.org/hco/18/GRCh38#69796779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89376025-C-A

69797400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89375007-A-T

69797441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89374965-G-A

69797562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89374634-T-C

http://identifiers.org/hco/18/GRCh38#69797712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89374489-A-C

69797761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89374442-G-A

69798793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362435-T-C

69798895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362345-G-A

69799087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362163-T-C

69799110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362140-T-G

69799173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362091-G-A

69799220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362049-G-A

69799271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89362011-A-G

69799322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89361959-A-G

69799326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89361957-T-A

69799326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89361957-T-C

http://identifiers.org/hco/18/GRCh38#69799626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89361662-C-A

69799772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89361572-A-G

69799889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89361484-T-C

69800056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89360718-C-T

69800069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89360705-T-C

69800111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89360674-A-T

69800353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89360438-C-T

69800999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89357704-T-A

69801049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89357662-G-A

69801435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89356893-A-G

69801636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89356677-C-G

69801735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89356584-T-C

69801857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89355943-C-T

69802200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89355577-A-G

69802957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89355421-T-C

69803080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89355281-G-A

69803425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354997-T-A

69803547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354881-T-A

69804011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354753-A-T

69804148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354632-G-T

http://identifiers.org/hco/18/GRCh38#69804246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89354548-C-A

69804246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354548-C-T

http://identifiers.org/hco/18/GRCh38#69804254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89354540-C-A

69804254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354540-C-G

69804312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354479-T-C

69804438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89354367-G-C

69804529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89351474-G-T

69804740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89351263-T-C

69804983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89350968-T-C

69805000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89350951-G-A

69805622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89350331-A-G

69805866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89349432-C-T

69806183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89349002-T-C

69806351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348881-T-C

69806482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348747-G-A

69806613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348620-T-C

69806726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348509-G-T

69806873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348376-A-G

69806873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348376-A-T

69807011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348235-G-A

69807161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89348088-T-C

69811727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347649-T-C

69811827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347546-A-G

69815177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347347-G-A

69815212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347314-G-A

69815500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347048-A-G

69815534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347012-G-A

69815534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89347012-G-C

69815597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89346951-T-C

69815657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89346896-A-T

69815803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89346663-A-T

69815905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89346560-T-G

69815987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89346500-T-G

http://identifiers.org/hco/18/GRCh38#69816450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89346088-A-C

69817829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89345497-A-G

69818415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89345066-G-A

69818415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89345066-G-C

69818541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89344952-C-T

69818883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89344563-C-G

69818930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89344517-G-A

69818930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89344517-G-C

69820093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89343728-T-C

69820554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89343367-G-A

69821574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342796-A-T

69821749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342611-G-T

http://identifiers.org/hco/18/GRCh38#69821765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89342595-A-C

69821765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342595-A-T

69821822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342539-T-C

69822298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342099-A-T

69822315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89342082-T-G

69822433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89341953-G-T

69827592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89335771-A-G

69827938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89335438-A-G

69828008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89335391-T-C

69828026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89335373-T-C

69828288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89328538-T-C

69828832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89328033-A-G

http://identifiers.org/hco/18/GRCh38#69828929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#89327954-A-C

69828929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89327954-A-G

69828929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89327954-A-T

69828991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89327893-T-A

69829589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89326696-G-A

69831066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron variant
orthologous variants: 89325413-C-T

69831205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 89325306-G-A

http://identifiers.org/hco/18/GRCh38#69831262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89325254-C-A

69831465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89325076-A-G

69835572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89324525-T-C

69835693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89324420-A-G

69836197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89323946-T-C

http://identifiers.org/hco/18/GRCh38#69836330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89323827-A-C

69836428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89323771-G-A

69836783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89323429-G-T

69839581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89321268-A-G

69840206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320570-G-T

69840344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320432-A-G

69840552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320251-A-G

http://identifiers.org/hco/18/GRCh38#69840560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89320243-A-C

69840628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320174-C-T

69840706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320099-G-A

69840758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: 89320049-T-G

http://identifiers.org/hco/18/GRCh38#69841102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89319694-C-A

69841327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 89319313-C-T

69841750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318893-G-T

http://identifiers.org/hco/18/GRCh38#69841863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89318781-C-A

69841863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318781-C-G

69841863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318781-C-T

http://identifiers.org/hco/18/GRCh38#69841880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89318762-A-C

69841880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318762-A-G

69841880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318762-A-T

69841899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318744-G-A

69841987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318638-A-G

69842036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318594-G-A

69842036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318594-G-T

69842108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318526-T-C

http://identifiers.org/hco/18/GRCh38#69842189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89318467-C-A

69842189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318467-C-G

69842223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89318431-G-C

69842347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 89318309-A-G

69843001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317687-A-G

69843013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317675-G-A

69843013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317675-G-C

69843013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317675-G-T

69843329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317357-T-C

69843507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317183-G-A

69843507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89317183-G-T

http://identifiers.org/hco/18/GRCh38#69843717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89316982-C-A

http://identifiers.org/hco/18/GRCh38#69843749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89316942-A-C

69843756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89316935-C-T

69844450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89316302-T-C

69845068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89315662-T-C

http://identifiers.org/hco/18/GRCh38#69845442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89315264-C-A

69845442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89315264-C-T

69845590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89315141-G-T

69846049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314721-C-T

69846098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314676-G-T

69846225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314547-A-G

69846284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314483-G-T

69846370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314410-G-A

69846370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314410-G-T

69846441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314341-C-T

http://identifiers.org/hco/18/GRCh38#69846541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89314243-A-C

69846541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89314243-A-G

69847001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89313809-C-G

69847014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89313796-G-C

69847299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89313580-G-A

69847299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89313580-G-T

69847757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89313105-T-A

69847899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312958-A-G

69847929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312930-G-A

69847929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312930-G-T

http://identifiers.org/hco/18/GRCh38#69847993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#89312880-C-A

69847993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312880-C-T

69848194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312700-T-C

69848396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312506-G-T

69848421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312481-A-G

69848738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312175-T-C

69848885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28301
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89312019-C-T